疾病名称 |
别名 |
|
Insulin-Like Growth Factor I |
Insulin-Like Growth Factor I Deficiency
|
IGF1 DEFICIENCY
|
Insulin-Like Growth Factor I, Resistance To
|
Growth Retardation With Deafness And Mental Retardation Due To Igf1 Deficiency
|
Growth Delay Due To Insulin-Like Growth Factor Type 1 Deficiency
|
Growth Delay Due To Insulin-Like Growth Factor I Resistance
|
IGF1RES
|
Igf-I Resistance
|
Somatomedin, End-Organ Insensitivity To
|
Somatomedin-C
|
Somatomedin-C, Resistance To
|
Growth Retardation With Sensorineural Deafness And Mental Retardation
|
Insulin-Like Growth Factor 1 Resistance To
|
Igf-1 Resistance
|
Somatomedin End-Organ Insensitivity To
|
Somatomedin-C Resistance To
|
Growth Restriction With Sensorineural Deafness And Intellectual Disability
|
Growth Delay-Deafness-Intellectual Disability Syndrome
|
Growth Delay-Hearing Loss-Intellectual Disability Syndrome
|
Igf-1 Deficiency
|
Primary Insulin-Like Growth Factor Deficiency
|
Resistance To Igf-1
|
Insulin-Like Growth Factor 1 Resistance
|
End-Organ Insensitivity To Somatomedin
|
Igf1 Resistance
|
Resistance To Insulin-Like Growth Factor I
|
Resistance To Somatomedin-C
|
Insulin-Like Growth Factor 1, Resistance To
|
|
|
Acromegaly |
Gigantism
|
Growth Hormone Excess
|
Pituitary Giant
|
Somatotroph Adenoma
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
|
Acid-Labile Subunit Deficiency |
Short Stature Due To Primary Acid-Labile Subunit Deficiency
|
ACLSD
|
Acid-Labile Subunit, Deficiency Of
|
Decreased Levels Of Acid Labile Subunit
|
Growth Disorders
|
|
|
Pituitary Gland Disease |
Pituitary Diseases
|
Pituitary Dysfunction
|
Pituitary Disease
|
Pituitary Deficiency
|
Pituitary Disorders
|
|
|
Laron Syndrome |
Growth Hormone Insensitivity Syndrome
|
Growth Hormone Receptor Deficiency
|
Laron Dwarfism
|
Pituitary Dwarfism Ii
|
Laron-Type Isolated Somatotropin Defect
|
Primary Growth Hormone Resistance
|
Laron-Type Dwarfism
|
Laron Type Pituitary Dwarfism I
|
Primary Growth Hormone Insensitivity
|
Primary Gh Resistance
|
Gh-R Deficiency
|
Growth Hormone Receptor Defect
|
Laron-Type Pituitary Dwarfism
|
Laron-Type Short Stature
|
Severe Gh Insensitivity
|
Ghis
|
Short Stature Due To A Defect In Growth Hormone Receptor Or Post-Receptor Pathway
|
Complete Growth Hormone Insensitivity
|
Gh Receptor Deficiency
|
Primary Gh Insensitivity
|
Short Stature Due To Growth Hormone Resistance
|
LARS
|
|
|
Protein-Energy Malnutrition |
PEM
|
Protein Energy Malnutrition
|
|
|
Aging |
|
|
Hypopituitarism |
Pituitary Hypofunction
|
Pituitary Insufficiency
|
Pituitary Hormone Deficiency
|
Subpituitarism
|
Hypophyseal Dystrophy
|
Hypohypophysism
|
Anterior Pituitary Insufficiency
|
Deficient Secretion Of One Or More Pituitary Hormones
|
Hypopituitarism Syndrome
|
Pituitary Deficiency
|
Pituitary Failure
|
Pituitary Insufficiency Nos
|
Anterior Pituitary Hypofunction
|
Deficient Secretion Of All Pituitary Hormones
|
Hypopituitary Dwarfism
|
Hyposomatotropic Dwarfism
|
Hypophyseal Dwarfism
|
Hypopituitary Cachexia
|
Hypophyseal Short Stature
|
Panhypopituitarism Syndrome
|
Pituitary Cachexia
|
Juvenile Hypopituitarism
|
Pituitary Dwarfism
|
Pituitary Gland Hypofunction
|
Primary Hypopituitarism
|
Secondary Hypogonadism
|
Prepubertal Panhypopituitarism
|
Prepubertal Dwarfism
|
Postpartum Panhypopituitary Syndrome
|
Postpartum Hypopituitarism
|
Pituitary Short Stature
|
Pituitary Infantilism
|
Pituitary Hypogonadism
|
Pituitary Hypoadrenocorticism
|
|
|
Turner Syndrome |
Monosomy X
|
Gonadal Dysgenesis Turner Type
|
Ullrich-Turner Syndrome
|
Bonnevie-Ullrich Syndrome
|
Karyotype 45, X
|
Genital Dwarfism, Turner Type
|
Gonadal Dysgenesis
|
45,X
|
Turner'S Syndrome
|
Gonadal Dysgenesis - Turner
|
Monosomy X Syndrome
|
Xo Syndrome
|
Genital Dwarfism
|
45, X Syndrome
|
Bonnevie-Ulrich Syndrome
|
Chromosome X Monosomy X
|
Schereshevkii Turner Syndrome
|
Turner Varny Syndrome
|
Ts
|
45,X Syndrome
|
45,X/46,Xx Syndrome
|
Turners Syndrome
|
Gonadal Dysgenesis, 45,X
|
X0 Syndrome
|
|
|
Anorexia Nervosa |
Anorexia Nervosa, Susceptibility To
|
ANON
|
Anorexia Nervosa, Susceptibility To, 1
|
An
|
Anorexia Nervosa 1
|
An - [Anorexia Nervosa]
|
|
|
Hyperinsulinism |
|
|
Hyperpituitarism |
|
|
Osteoporosis |
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
OSTEOP
|
Involutional Osteoporosis
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
Type 1 Osteoporosis
|
|
|
Hyperprolactinemia |
Chiari-Frommel Syndrome
|
Hyperprolactinaemia
|
Familial Hyperprolactinemia
|
HPRL
|
Pregnancy-Related A-G Syndrome
|
Familial Isolated Prolactin Receptor Deficiency
|
|
|
Craniopharyngioma |
Neoplasm Of Rathke'S Pouch
|
Adamantinomatous Tumor
|
Craniopharyngeal Duct Tumor
|
Dysodontogenic Epithelial Tumor
|
Rathke'S Pouch Tumor
|
|
|
Donohue Syndrome |
Leprechaunism
|
Leprechaunism Syndrome
|
Donohue'S Syndrome
|
LEPRCH
|
|
|
Anovulation |
|
|
Hyperandrogenism |
Hyperandrogenization Syndrome
|
|
|
Polycystic Ovary Syndrome |
Polycystic Ovarian Syndrome
|
Pcos
|
Polycystic Ovarian Disease
|
Polycystic Ovaries
|
Stein-Leventhal Syndrome
|
Multicystic Ovaries
|
Polycystic Ovary
|
Sclerocystic Ovaries
|
Sclerocystic Ovary Syndrome
|
Stein-Leventhal Synd.
|
Cystic Disease Of Ovaries
|
Cystic Disease Of Ovary
|
Pco
|
Pcod
|
Sclerocystic Ovarian Degeneration
|
Polycystic Ovary Syndrome, Susceptibility To
|
Pcos - [Polycystic Ovary Syndrome]
|
Polycystic Ovary Nos
|
Pco - [Polycystic Ovary]
|
|
|
Sheehan Syndrome |
Postpartum Hypopituitarism
|
Sheehan'S Syndrome
|
Postpartum Panhypopituitarism
|
Postpartum Panhypopituitary Syndrome
|
Postpartum Pituitary Necrosis
|
Simmond'S Disease
|
|
|
Glucose Intolerance |
Glucose: Intolerance
|
Glucose: Malabsorption
|
Malabsorption Of Glucose
|
Impaired Glucose Tolerance
|
|
|
Prolactinoma |
Prolactin-Producing Pituitary Gland Adenoma
|
Prolactin-Secreting Pituitary Adenoma
|
Forbes-Albright Syndrome
|
Lactotroph Adenoma
|
Prl-Secreting Pituitary Adenoma
|
Prloma
|
Pituitary Lactotrophic Adenoma
|
Familial Prolactinoma
|
Pituitary Adenoma, Prolactin-Secreting
|
Prolactinoma Of Pituitary Gland
|
PSPA
|
|
|
Ovarian Disease |
Ovarian Dysfunction
|
Ovarian Diseases
|
Ovarian Disorders
|
Disorder Of Endocrine Ovary
|
|
|
Muscle Hypertrophy |
MSLHP
|
Hypertrophy
|
Hypertrophy, Muscle
|
|
|
Empty Sella Syndrome |
Empty Sella Turcica
|
Empty Sella
|
|
|
Peho Syndrome |
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy
|
Infantile Cerebellooptic Atrophy
|
PEHO
|
Progressive Encephalopathy With Edema, Hypsarrhythmia And Optic Atrophy
|
Progressive Encephalopathy-Optic Atrophy Syndrome
|
|
|
Osteoporosis, Juvenile |
Idiopathic Juvenile Osteoporosis
|
Idiopathic Osteoporosis
|
Juvenile Osteoporosis
|
Ijo
|
|
|
Nutritional Deficiency Disease |
Malnutrition
|
Nutritional Disorder
|
Nutritional Deficiency
|
Nutrition
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
Nutrition Disorders
|
|
|
Hyperglycemia |
|
|
Pituitary Tumors |
Pituitary Tumor
|
Pituitary Neoplasms
|
|
|
Cerebral Meningioma |
|
|
Pituitary Hormone Deficiency, Combined, 2 |
Panhypopituitarism
|
Combined Pituitary Hormone Deficiency
|
CPHD2
|
Ateliotic Dwarfism With Hypogonadism
|
Pituitary Dwarfism Iii
|
Hanhart Dwarfism
|
Simmond'S Disease
|
Simmonds' Disease
|
Cphd
|
Pituitary Hormone Deficiency, Combined
|
Hormone Deficiency, Pituitary, Combined, Type 2
|
Pituitary Dwarfism Type 3
|
Sheehan Syndrome
|
|
|
Mccune-Albright Syndrome |
Mass Syndrome
|
Polyostotic Fibrous Dysplasia
|
MAS
|
Fibrous Dysplasia Of Bone
|
Albright Syndrome
|
Mass Phenotype
|
Overlap Connective Tissue Disease
|
Mccune Albright Syndrome
|
Osteitis Fibrosa Disseminata
|
OCTD
|
Albright'S Disease
|
Pfd
|
Pofd
|
Albright'S Syndrome
|
Mccune-Albright Syndrome, Somatic, Mosaic
|
Albright'S Disease Of Bone
|
Albright'S Syndrome With Precocious Puberty
|
Albright-Mccune-Sternberg Syndrome
|
Albright-Sternberg Syndrome
|
Fibrous Dysplasia With Pigmentary Skin Changes And Precocious Puberty
|
Gonadotropin-Independent Female-Limited Sexual Precocity
|
Fibrous Dysplasia Polyostotic
|
Fibrous Dysplasia, Polyostotic
|
|
|
Pituitary Adenoma 1, Multiple Types |
Pituitary Adenoma Predisposition
|
PITA1
|
Isolated Familial Somatotropinoma
|
Fis
|
Ifs
|
Somatotrophinoma, Familial
|
Acromegaly Due To Pituitary Adenoma 1
|
Pagh1
|
Pituitary Adenoma 1
|
Somatotropinoma, Familial Isolated
|
Somatotropic Adenoma
|
Somatotropinoma
|
Pituitary Gigantism
|
Hypophyseal Gigantism
|
Infantile And Juvenile Forms Of Acromegaly
|
Acromegaly Due To Pituitary Adenoma
|
Familial Isolated Pituitary Adenoma
|
Familial Isolated Somatotropinomas
|
Familial Somatotrophinoma
|
Fipa
|
Pituitary Adenoma, Growth Hormone-Secreting, 1
|
Gigantism Pituitary
|
Pituitary Adenoma, Type 1, Multiple Types
|
Gigantism
|
Pituitary Adenoma, Familial Isolated
|
Multiple Gastrointestinal Atresias
|
|
|
Microvascular Complications Of Diabetes 1 |
Proliferative Diabetic Retinopathy
|
Microvascular Complications Of Diabetes, Susceptibility To, 1
|
MVCD1
|
Diabetic Nephropathy
|
Non-Proliferative Diabetic Retinopathy
|
Nonproliferative Diabetic Retinopathy
|
Proliferative Retinopathy, Diabetic
|
Proliferative Retinopathy, Diabetic, Susceptibility To
|
Nonproliferative Retinopathy, Diabetic
|
Nonproliferative Retinopathy, Diabetic, Susceptibility To
|
Pdr
|
Diabetic End-Stage Renal Disease
|
Diabetic Neuropathy
|
Diabetic Neuropathies
|
Complications Of Diabetes Mellitus
|
Diabetes Mellitus, Independent Of Type With Proliferative Retinopathy
|
|
|
Pituitary Adenoma |
Adenoma Of The Pituitary Gland
|
Pituitary Adenomas
|
Adenoma, Pituitary
|
Pituitary Gland Adenoma
|
Pituitary Neoplasms
|
|
|
Adenoma |
Acinar Cell Adenoma
|
Adenomas
|
Acinic Cell Adenoma
|
|
|
Hypogonadism |
|
|
Hypoglycemia |
Hypoglycaemia
|
Low Blood Sugar
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
Hypoglycaemic Syndrome
|
|
|
Prediabetes Syndrome |
Prediabetes
|
Impaired Glucose Tolerance
|
Prediabetic State
|
IGT
|
Igt - [Impaired Glucose Tolerance]
|
Impaired Glucose Tolerance With Unspecified Complication
|
Impaired Glucose Tolerance Without Complication
|
Abnormal Glucose Tolerance
|
|
|
Type 1 Diabetes Mellitus |
Diabetes Mellitus, Insulin-Dependent
|
Diabetes Mellitus Type 1
|
IDDM
|
Type 1 Diabetes
|
Insulin-Dependent Diabetes Mellitus
|
T1D
|
Juvenile-Onset Diabetes
|
Jod
|
Diabetes Mellitus, Type 1
|
Diabetes Mellitus, Insulin-Dependent-1
|
Type I Diabetes Mellitus
|
Autoimmune Diabetes
|
Juvenile Diabetes
|
Juvenile-Onset Diabetes Mellitus
|
Diabetes, Insulin Dependent
|
Insulin-Dependent Diabetes Mellitus-1
|
Diabetes Mellitus Insulin-Dependent
|
Diabetes Autoimmune
|
Diabetes Mellitus, Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 1, Susceptibility To
|
Diabetes Type 1
|
Type I Diabetes
|
Diabetes, Autoimmune
|
T1dm - [Type 1 Diabetes Mellitus]
|
Iddm - [Insulin Dependent Diabetes Mellitus]
|
Type 1 Iddm
|
Juvenile Diabetes Mellitus Without Compications
|
Idiopathic Insulin-Dependent Diabetes Mellitus Without Complications
|
Juvenile-Onset Diabetes Mellitus Without Compications
|
Ketosis-Prone Diabetes Mellitus Without Compications
|
Juvenile-Onset-Type Diabetes Mellitus Without Compications
|
|
|
Prader-Willi Syndrome |
Prader-Labhart-Willi Syndrome
|
PWS
|
Willi-Prader Syndrome
|
Prader-Willi Syndrome Due To Translocation
|
Prader-Willi Syndrome Due To Imprinting Mutation
|
Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15
|
Prader Willi Syndrome
|
Upd(15)Mat
|
|
|
Fibrous Dysplasia |
Fibrous Dysplasia Of Bone
|
|
|
Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities |
Rabson-Mendenhall Syndrome
|
Mendenhall Syndrome
|
Pineal Hyperplasia And Diabetes Mellitus Syndrome
|
RMS
|
Leprechaunism
|
Insr-Related Severe Syndromic Insulin Resistance
|
Donohue Syndrome
|
|
|
Chronic Kidney Disease |
Chronic Renal Disease
|
Chronic Kidney Failure
|
Ckd
|
Chronic Renal Failure
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
Crf
|
Renal Failure - Chronic
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
Endometrial Cancer |
Endometrial Carcinoma
|
Endometrial Neoplasm
|
Malignant Neoplasm Of Endometrium
|
Endometrioid Carcinoma
|
Endometrial Neoplasms
|
Carcinoma, Endometrioid
|
Endometrial Cancer, Familial
|
Endometrial Carcinoma, Somatic
|
Endometrial Cancer, Susceptibility To
|
Endometrial Ca
|
Malignant Endometrial Neoplasm
|
Neoplasm Of Endometrium
|
Primary Malignant Neoplasm Of Endometrium
|
Tumor Of Endometrium
|
Carcinoma Of The Endometrium
|
Endometrioid Carcinoma Of Female Reproductive System
|
ENDMC
|
Carcinoma Endometrioid
|
Endometrial Cancers
|
Cancer, Endometrial
|
Uterine Corpus Cancer
|
|
|
Skin Tag |
Fibroepithelial Polyp
|
Fibroepithelial Polyp Of Skin
|
Soft Fibroma
|
Skin Tags
|
Cutaneous Tag
|
Gardner Fibroma
|
Acrochordon
|
Fibroma Molle
|
|
|
Fetal Macrosomia |
|
|
Type 2 Diabetes Mellitus |
Insulin Resistance
|
NIDDM
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
Dm Type Ii
|
Diabetic Type 2
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
Stable Diabetes
|
|
|
Chronic Fatigue Syndrome |
Myalgic Encephalomyelitis
|
Postviral Fatigue Syndrome
|
Cfs
|
Myalgic Encephalitis
|
Encephalomyelitis, Myalgic
|
Chronic Fatigue
|
Fatigue Syndrome, Chronic
|
Benign Myalgic Encephalomyelitis
|
Akureyri
|
Akureyri Disease
|
Cfs - [Chronic Fatigue Syndrome]
|
Epidemic Neuromyasthenia
|
Myalgic Encephalomyelitis Syndrome
|
Me - [Myalgic Encephalomyelitis]
|
Pvfs - [Postviral Fatigue Syndrome]
|
Neuromyasthenia
|
Iceland Disease
|
Icelandic Disease
|
|
|
Amenorrhea |
Absence Of Menstruation
|
Amenia
|
|
|
Pituitary Infarct |
|
|
Breast Disease |
|
|
Galactorrhea |
Galactorrhea Not Associated With Childbirth
|
Galactorrhea Associated With Childbirth
|
|
|
Acne |
Acne Vulgaris
|
Acne Varioliformis
|
Frontalis Acne
|
|
|
Sleep Apnea |
|
|
Hypothyroidism |
Thyroid Diseases
|
Thyroid Disease
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
Achondroplasia |
Achondroplastic Dwarfism
|
ACH
|
Osteosclerosis Congenita
|
Achondroplastic Physique
|
Chondrodystrophia
|
Dwarf, Achondroplastic
|
Achondroplastic Short Stature
|
Congenital Osteosclerosis
|
|
|
Hyperostosis |
Hypertrophy Of Bone
|
Bone Hypertrophy
|
Bone Thickening
|
Periosteum Thickening
|
|
|
Short Bowel Syndrome |
Short Gut Syndrome
|
Acquired Short Bowel Syndrome
|
Secondary Short Bowel Syndrome
|
Short Bowel Nos
|
|
|
Renal Osteodystrophy |
Renal Rickets
|
Chronic Kidney Disease-Mineral And Bone Disorder
|
|
|
Isolated Growth Hormone Deficiency, Type Ia |
Ighd Ia
|
Primordial Dwarfism
|
Isolated Growth Hormone Deficiency Type Ia
|
Sexual Ateleiotic Dwarfism
|
Pituitary Dwarfism I
|
IGHD1A
|
Illig-Type Growth Hormone Deficiency
|
Growth Hormone Deficiency, Isolated, Type Ia
|
Congenital Ighd Type Ia
|
Congenital Isolated Gh Deficiency Type Ia
|
Congenital Isolated Growth Hormone Deficiency Type Ia
|
Pituitary Dwarfism 1
|
Growth Hormone Deficiency, Isolated, Autosomal Recessive
|
Autosomal Recessive Isolated Growth Hormone Deficiency
|
Isolated Growth Hormone Deficiency Type 1a
|
Congenital Ighd
|
Congenital Isolated Gh Deficiency
|
Congenital Isolated Growth Hormone Deficiency
|
Growth Hormone Deficiency, Isolated Autosomal Recessive
|
Illig Type Growth Hormone Deficiency
|
Non-Acquired Isolated Growth Hormone Deficiency
|
Growth Hormone Deficiency, Isolated, 1a
|
Growth Hormone Deficiency Isolated Autosomal Recessive
|
Dwarfism, Primordial
|
Dwarfism
|
|
|
Nerve Compression Syndrome |
Entrapment Neuropathies
|
Compression Neuropathy
|
Entrapment Neuropathy
|
Peripheral Nerve Entrapment Syndrome
|
Nerve Compression Syndromes
|
Hereditary Liability To Pressure Palsies
|
|
|
Microvascular Complications Of Diabetes 5 |
Diabetic Retinopathy
|
Microvascular Complications Of Diabetes, Susceptibility To, 5
|
MVCD5
|
Retinopathy, Diabetic
|
Diabetic Nephropathy
|
Retinopathy, Diabetic, Susceptibility To
|
Retinal Abnormality - Diabetes-Related
|
|
|
Sotos Syndrome |
Cerebral Gigantism
|
SOTOS
|
Chromosome 5q35 Deletion Syndrome
|
Sotos Syndrome 1, Formerly
|
Sotos1, Formerly
|
Distinctive Facial Appearance, Overgrowth In Childhood, And Learning Disabilities Or Delayed Development
|
Sotos Sequence
|
Sotos' Syndrome
|
Sotos1
|
Sotos Syndrome 1
|
|
|
Goiter |
|
|
Pseudohypoparathyroidism |
Familial Pseudohypoparathyroidism
|
Parathyroid Hormone Resistant Hypoparathyroidism
|
Php - [Pseudohypoparathyroidism]
|
Constitutional Chronic Hypocalcaemia
|
|
|
Metabolic Acidosis |
|
|
Fibromyalgia |
Diffuse Myofascial Pain Syndrome
|
Fibromyalgia Syndrome
|
Fibromyalgia-Fibromyositis Syndrome
|
Fibromyositis
|
Fibrositis
|
Fms
|
Myofascial Pain Syndrome
|
Myofascial Pain Syndromes
|
|
|
Hyperthyroidism |
|
|
Pancreatic Adenocarcinoma |
Adenocarcinoma Of The Pancreas
|
Adenocarcinoma Of Pancreas
|
Pancreas Adenocarcinoma
|
Malignant Exocrine Neoplasm
|
Primary Pancreatic Adenocarcinoma
|
Adenocarcinoma Of Islet Cell Of Pancreas
|
Islet Cell Adenocarcinoma Of Unspecified Site
|
Mixed Adenocarcinoma Islet Cell With Exocrine Of Unspecified Site
|
|
|
Intermittent Claudication |
Charcot'S Syndrome
|
Amyotrophic Lateral Sclerosis
|
|
|
Acanthosis Nigricans |
|
|
Arthropathy |
Ankylosis Of Ankle And Foot Joint
|
Ankylosis Of Forearm Joint
|
Ankylosis Of Hand Joint
|
Ankylosis Of Joint Of Ankle And/Or Foot
|
Ankylosis Of Joint Of Forearm
|
Ankylosis Of Joint Of Hand
|
Ankylosis Of Joint Of Lower Leg
|
Ankylosis Of Joint Of Multiple Sites
|
Ankylosis Of Joint Of Pelvic Region And Thigh
|
Ankylosis Of Joint Of Shoulder Region
|
Ankylosis Of Joint Of Upper Arm
|
Ankylosis Of Lower Leg Joint
|
Ankylosis Of Multiple Joints
|
Ankylosis Of Upper Arm Joint
|
Infectious Arthropathy
|
Joint Ankylosis Of The Ankle And Foot
|
Joint Ankylosis Of The Ankle And/Or Foot
|
Joint Ankylosis Of The Forearm
|
Joint Ankylosis Of The Hand
|
Joint Ankylosis Of The Lower Leg
|
Joint Ankylosis Of The Pelvic Region And Thigh
|
Joint Ankylosis Of The Shoulder Region
|
Joint Ankylosis Of The Upper Arm
|
Joint Diseases
|
Joint Disease
|
Arthropathy Associated With Infection
|
|
|
Pineal Region Choriocarcinoma |
|
|
Congenital Hypothyroidism |
Cretinism
|
Neonatal Hypothyroidism
|
Ch
|
Cht
|
Congenital Myxedema
|
Myxedema, Congenital
|
Endemic Cretinism
|
Congenital Iodine-Deficiency Syndrome
|
Fetal Iodine Deficiency Syndrome
|
Congenital Iodine-Deficiency Hypothyroidism Nos
|
|
|
Breast Cancer |
Breast Carcinoma
|
Male Breast Cancer
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
Mammary Cancer
|
Mammary Tumor
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
Familial Breast Cancer
|
Cancer Of Breast
|
BC
|
Breast Cancer Familial
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
Breast Male Carcinoma
|
Breast Neoplasms
|
Breast Neoplasms, Male
|
Mammary Tumors
|
Mammary Carcinomas
|
Cancer, Breast
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
Carcinoma With Apocrine Differentiation
|
|
|
Diabetes Mellitus |
|
|
Pyloric Stenosis |
|
|
Portal Hypertension |
Hypertension, Portal
|
Hypertension Portal
|
Pht - [Portal Hypertension]
|
Portal Htn
|
|
|
Acidophil Adenoma |
Adenoma, Acidophil
|
Eosinophil Adenoma
|
|
|
Conn'S Syndrome |
Cushing Syndrome
|
Hyperaldosteronism
|
Primary Hyperaldosteronism
|
Hypercortisolism
|
Primary Aldosteronism
|
Cushing'S Syndrome
|
Adrenal Gland Hyperfunction
|
Conn Syndrome
|
Hyperadrenalism
|
Ectopic Acth Syndrome
|
Hyperadrenocorticism
|
Cushing Disease
|
Cushing'S Disease
|
Adrenal Cortex Adenoma
|
Corticotroph Pituitary Adenoma
|
Pituitary Corticotroph Micro-Adenoma
|
Pituitary-Dependent Cushing Syndrome
|
Pituitary Acth Hypersecretion
|
Acth Syndrome, Ectopic
|
Acth-Secreting Pituitary Adenoma
|
Adrenal Hyperfunction Resulting From Pituitary Acth Excess
|
Ectopic Adrenocorticotropic Hormone Syndrome
|
Nodular Primary Adrenocortical Dysplasia
|
Pituitary Dependent Cushing Syndrome
|
Pituitary Cushing Syndrome
|
Pituitary-Dependant Cushing Syndrome
|
Pituitary-Dependant Hypercortisolism
|
Pituitary-Dependant Hypercortisolism Disorder
|
Aldosteronism Primary
|
Acth Syndrome Ectopic
|
Adrenal Cushing'S Syndrome
|
Adrenal Cortical Adenoma
|
Cushing Syndrome Nos
|
Cortisol Hypersecretion
|
Corticoadrenal Hypersecretion
|
Cushing Syndrome Secondary To Ectopic Acth-Secretion
|
Ectopic Cushing Syndrome
|
Hypercortisolism Due To Nonpituitary Tumour
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
|
Idiopathic Aldosteronism
|
Aldosteronism
|
Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia
|
Primary Aldosteronism Due To Adrenal Hyperplasia
|
|
|
Hyperparathyroidism |
Hyperparathyroidism And Other Disorders Of Parathyroid Gland
|
Parathyroid Hyperfunction
|
Hpth - [Hyperparathyroidism]
|
Parathyroid Gland Hyperfunction
|
Parathyroid Glandular Hyperfunction
|
|
|
Osteoarthritis |
Osteoarthrosis
|
Degenerative Joint Disease
|
Hypertrophic Arthritis
|
Arthropathy
|
Degenerative Polyarthritis
|
Degenerative Arthritis
|
Osteoarthrosis And Allied Disorder
|
Arthritis, Degenerative
|
Oa
|
Osteoarthritis Deformans
|
Osteoarthrosis Deformans
|
Kashin-Beck Disease
|
|
|
Pituitary Cancer |
Pituitary Carcinoma
|
Malignant Pituitary Neoplasm
|
Malignant Tumor Of Pituitary Gland
|
Neoplasm Of Pituitary Gland
|
Pituitary Gland Cancer
|
Pituitary Gland Neoplasm
|
Pituitary Neoplasm
|
Carcinoma Of The Pituitary Gland
|
Neoplasm Of The Pituitary Gland
|
Pituitary Neoplasms
|
Malignant Neoplasm Of Pituitary Gland
|
|
|
Rickets |
Vitamin D Deficiency
|
Vitamin D
|
Active Rickets
|
Hypovitaminosis D
|
Nutritional Rickets
|
Vitamin D Deficiency Disease
|
Vitamin-D Deficiency Rickets
|
Vitamin D-Dependent Rickets
|
Avitaminosis D
|
Infantile Osteomalacia
|
Juvenile Osteomalacia
|
|
|
Embryonal Rhabdomyosarcoma |
Rhabdomyosarcoma, Embryonal
|
Rhabdomyosarcoma Embryonal
|
Botryoid Rhabdomyosarcoma
|
Erms
|
Spindle Cell Rhabdomyosarcomas
|
|
|
Potocki-Lupski Syndrome |
PTLS
|
Chromosome 17p11.2 Duplication Syndrome
|
17p11.2 Microduplication Syndrome
|
Duplication 17p11.2 Syndrome
|
Trisomy 17p11.2
|
Potocki-Lupski Syndrome (Dup(17)(P11.2p11.2))
|
17p11.2 Duplication Syndrome
|
Dup(17)(P11.2p11.2)
|
Pls
|
Chromosome 17, Trisomy 17p11 2
|
|
|
Prostate Cancer |
Prostate Carcinoma
|
Prostate Cancer, Familial
|
Prostate Neoplasm
|
Prostate Cancer, Somatic
|
Prostate Cancer, Susceptibility To
|
Prostatic Cancer
|
Prostatic Neoplasms
|
Hereditary Prostate Cancer
|
Prostatic Neoplasm
|
Cancer Of Prostate
|
Carcinoma Of Prostate
|
Familial Prostate Cancer
|
Familial Prostate Carcinoma
|
Malignant Tumor Of Prostate
|
Malignant Neoplasm Of Prostate
|
Prostate Cancer, Familial, Susceptibility To
|
Malignant Tumor Of The Prostate
|
Ngp - New Growth Of Prostate
|
Tumor Of The Prostate
|
Prostate Cancer, Hereditary
|
Cancer Of The Prostate
|
Malignant Neoplasm Of The Prostate
|
Prostatic Carcinoma
|
PC
|
Prca
|
Cancer, Prostate
|
Malignant Prostatic Tumour
|
Malignant Tumour Of Prostate
|
Primary Prostate Cancer
|
Primary Malignant Neoplasm Of Prostate
|
Prostate Gland Cancer
|
|
|
Bone Disease |
Bone Diseases
|
Skeletal Disease
|
Skeletal Disorder
|
Disorder Of Skeletal System
|
|
|
Exudative Vitreoretinopathy 1 |
Retinopathy Of Prematurity
|
Retrolental Fibroplasia
|
EVR1
|
Criswick-Schepens Syndrome
|
Rop
|
Exudative Vitreoretinopathy, Familial, Autosomal Dominant
|
Fevr, Autosomal Dominant
|
Premature Retinopathy
|
Vitreoretinopathy, Exudative 1
|
Autosomal Dominant Familial Exudative Vitreoretinopathy
|
Fevr
|
Vitreoretinopathy, Exudative, Type 1
|
Retinopathy Of Prematurity Nos
|
Rlf- [Retrolental Fibroplasia]
|
Rop - [Retinopathy Of Prematurity]
|
Terry Syndrome
|
|
|
Carcinoid Syndrome |
Carcinoid Tumor
|
Malignant Carcinoid Syndrome
|
Carcinoid Tumor Syndrome
|
Carcinoid Tumors
|
Carcinoid Tumor No Icd-O Subtype
|
Argentaffinoma Syndrome
|
|
|
Lymphangioleiomyomatosis |
Lymphangiomyomatosis
|
LAM
|
Lung Lymphangioleiomyomatosis
|
Pulmonary Lymphangioleiomyomatosis
|
Lymphangioleiomyomatosis, Somatic
|
Lymphangio-Myomatosis
|
|
|
Glycogen Storage Disease |
Glycogenosis
|
Glycogenoses
|
Gsd
|
Storage Disease, Glycogen
|
Gsd - [Glycogen Storage Disease]
|
Glycogen Thesaurismosis
|
Diffuse Glycogenosis
|
Generalised Glycogen Storage Disease
|
Generalised Glycogenosis
|
Generalised Glycogen Storage Disease Of Infants
|
Glycogen Synthase Deficiency
|
|
|
Functioning Pituitary Adenoma |
Secretory Adenoma Of The Pituitary Gland
|
Endocrine Active Pituitary Adenoma
|
Secreting Pituitary Adenoma
|
Pituitary Adenoma, Functioning
|
|
|
Gestational Diabetes |
Gestational Diabetes Mellitus
|
GDM
|
Diabetes Mellitus Arising In Pregnancy
|
Maternal Gestational Diabetes Mellitus
|
Diabetes Mellitus, Gestational
|
Diabetes Mellitus, Pregnancy Related
|
Diabetes, Pregnancy-Induced
|
Diabetes Gestational
|
Diabetes, Gestational
|
Diabetes Of Pregnancy
|
Gdm - [Gestational Diabetes Mellitus]
|
Gestational Diabetes Mellitus Nos
|
Gestational Diabetes Complicating Pregnancy, Childbirth, Or The Puerperium
|
|
|
Neuroendocrine Tumor |
Neuroendocrine Neoplasm
|
Neuroendocrine Tumors
|
Carcinoma, Neuroendocrine
|
|
|
Motor Neuron Disease |
Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
Creeping Palsy
|
Creeping Paralysis
|
Bulbar Motor Neuron Disease
|
Bulbar Syndrome
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
Noonan Syndrome 1 |
Noonan Syndrome
|
NS1
|
Male Turner Syndrome
|
Female Pseudo-Turner Syndrome
|
Turner Phenotype With Normal Karyotype
|
Noonan Syndrome With Pigmented Villonodular Synovitis
|
Turner'S Phenotype, Karyotype Normal
|
Familial Turner Syndrome
|
Noonan'S Syndrome
|
Noonan-Ehmke Syndrome
|
Ns
|
Pseudo-Ullrich-Turner Syndrome
|
Turner Syndrome In Female With X Chromosome
|
Turner-Like Syndrome
|
Ullrich-Noonan Syndrome
|
Noonan-Like/Multiple Giant Cell Lesion Syndrome
|
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
|
Pterygium Colli Syndrome
|
Noonan Syndrome, Type 1
|
Turner Syndrome, Male
|
|
|
Alopecia |
|
|
Diffuse Idiopathic Skeletal Hyperostosis |
Hyperostosis, Diffuse Idiopathic Skeletal
|
Ankylosing Vertebral Hyperostosis
|
Dish
|
Disseminated Idiopathic Skeletal Hyperostosis
|
Forestier Disease
|
Forestier'S Disease
|
Hyperostosis Diffuse Idiopathic Skeletal
|
|
|
Hormone Producing Pituitary Cancer |
Growth Hormone Producing Pituitary Tumor
|
Pituitary Tumors, Hormone Producing
|
Somatotropinoma
|
Growth Hormone-Producing Pituitary Gland Neoplasm
|
|
|
Rett Syndrome |
Atypical Rett Syndrome
|
RTT
|
Rett Disorder
|
Rts
|
Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use
|
Rett Syndrome, Preserved Speech Variant
|
Rett Syndrome, Atypical
|
Rett'S Disorder
|
Rett Syndrome Variant
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome
|
Cerebroatrophic Hyperammonemia
|
Rett Like Syndrome
|
Rett'S Syndrome
|
Atypical Rtt
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use
|
Rett Syndrome Preserved Speech Variant
|
Rett Syndrome Zappella Variant
|
Rett Syndrome, Zappella Variant
|
|
|
Asperger Syndrome |
Asperger Disorder
|
Asperger Syndrome, Susceptibility To
|
|
|
Leptin Deficiency Or Dysfunction |
Morbid Obesity
|
Obesity Due To Congenital Leptin Deficiency
|
LEPD
|
Congenital Leptin Deficiency
|
Obesity, Morbid
|
Obesity, Morbid, Due To Leptin Deficiency
|
Severe Obesity
|
Obesity, Morbid, Nonsyndromic 1
|
Leptin Deficiency
|
Obesity, Severe, Due To Leptin Deficiency
|
Leptin
|
Morbid Obesity Due To Leptin Deficiency
|
Obesity Morbid
|
Leptin Dysfunction
|
|
|
Retinal Detachment |
Retinal Detachments
|
Rhegmatogenous Retinal Detachment
|
Ruptured Retina With Detachment
|
Retinal Hole With Detachment
|
|
|
Tuberous Sclerosis |
Tuberous Sclerosis Syndrome
|
Bourneville'S Disease
|
Epiloia
|
Cerebral Sclerosis
|
Tuberose Sclerosis
|
Tuberous Sclerosis 1
|
Bourneville Disease
|
Bourneville Phakomatosis
|
Pringle'S Disease
|
|
|
Body Mass Index Quantitative Trait Locus 11 |
OBESITY
|
Obesity, Susceptibility To
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
Obesity , Susceptibility To
|
BMIQ11
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
Simple Obesity Nos
|
Excess Fat
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
Interstitial Lung Disease |
Ild
|
Lung Diseases, Interstitial
|
Lung Diseases Interstitial
|
Interstitial Lung Diseases
|
|
|
Sebaceous Gland Disease |
Sebaceous Gland Anomaly
|
Sebaceous Gland Diseases
|
|
|
Beta-Thalassemia |
Beta Thalassemia
|
Cooley'S Anemia
|
Mediterranean Anemia
|
Beta Thalassemia Intermedia
|
Erythroblastic Anemia
|
Thalassemia, Hispanic Gamma-Delta-Beta
|
Thalassemia Major
|
Thalassemia Minor
|
Beta-Plus-Thalassemia
|
Thalassemia, Beta
|
Beta Thalassemia Major
|
Beta Thalassemia Minor
|
Thalassemias, Beta-
|
Microcytemia, Beta Type
|
Thalassemia, Beta Type
|
B-THAL
|
Mediterranean Anaemia
|
Beta Thalassaemia Syndrome
|
Mediterranean Disease
|
Beta Thalassaemia Disease
|
|
|
Mixed Cell Adenoma |
|
|
Acquired Immunodeficiency Syndrome |
Acquired Immune Deficiency Syndrome
|
AIDS
|
Acquired Immune Deficiency
|
Acquired Immunodeficiency
|
Acquired Immunodeficiency Due To Protein Loss
|
|
|
Non-Alcoholic Fatty Liver Disease |
Fatty Liver
|
Non-Alcoholic Fatty Liver
|
Nafld
|
Nonalcoholic Fatty Liver Disease
|
Nonalcoholic Steatohepatitis
|
Steatosis
|
Nafl
|
Nash
|
Non-Alcoholic Steatohepatitis
|
Susceptibility To Nonalcoholic Fatty Liver Disease
|
Steatohepatitis
|
Fatty Degeneration
|
Non-Alcoholic Fatty Liver Disease Without Mention Of Non-Alcoholic Steatohepatitis
|
Nafld Without Nash
|
Nafld Without Mention Of Nash
|
|
|
Ewing Sarcoma |
Neuroepithelioma
|
Ewing'S Tumor
|
Primitive Neuroectodermal Tumor
|
Ewings Sarcoma
|
Ewing'S Sarcoma
|
Peripheral Neuroepithelioma
|
ES
|
Ewings Sarcoma-Primitive Neuroectodermal Tumor
|
Localized Peripheral Primitive Neuroectodermal Tumor
|
Peripheral Primitive Neuroectodermal Tumor
|
Ewing Tumor
|
Sarcoma, Ewing'S
|
Ewing Family Of Tumors
|
Extraosseous Ewing Tumor
|
Askin Tumor
|
Ewing'S Family Localized Tumor
|
Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor
|
Localized Ewing Sarcoma
|
Localized Ewing'S Sarcoma
|
Localized Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor
|
Localized Ewing'S Tumor
|
Pnet Of Thoracopulmonary Region
|
Tumor Of The Ewing Family
|
Skeletal Ewing Sarcoma
|
Osseous Ewing Sarcoma
|
Ppnet
|
Peripheral Pnet
|
Extraskeletal Ewing Sarcoma
|
Eoe
|
Extraosseous Ewing Sarcoma
|
Extraskeletal Ewing Tumor
|
Esft
|
Ewing Sarcoma Family Of Tumors
|
Pne
|
Pnet
|
Pnet Of The Chest Wall
|
Sarcoma, Ewing
|
Neuroectodermal Tumors, Primitive, Peripheral
|
Neuroectodermal Tumor, Primitive
|
Disorder Of Eye
|
Askin'S Tumor
|
Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor
|
Neuroepithelioma, Peripheral
|
|
|
Adermatoglyphia |
ADERM
|
Immigration Delay Disease
|
Absence Of Fingerprints
|
Adg
|
Congenital Absence Of Fingerprints
|
Isolated Congenital Adermatoglyphia
|
Fingerprints, Absence Of
|
Skin Abnormalities
|
|
|
Cardiovascular System Disease |
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
Cardiovascular Diseases
|
|
|
Thalassemia |
Sickle-Cell Thalassemia With Crisis
|
Sickle-Cell Thalassemia Without Crisis
|
Thalassemia Hb-S Disease With Crisis
|
Thalassemia Hb-S Disease Without Crisis
|
Thalassemias
|
Hereditary Leptocytosis
|
Haemoglobin Thalassaemia Disorder
|
Thalassaemia Syndrome
|
Thalassaemia Nos
|
Thalassemia Variants
|
|
|
Pituitary Apoplexy |
|
|
Fatty Liver Disease |
Alcoholic Fatty Liver
|
Fatty Liver
|
Fatty Liver, Alcoholic
|
Fatty Change Of Liver
|
Hepatic Lipidosis
|
Steatosis Of Liver
|
Fatty Liver Alcoholic
|
Steatohepatitis
|
Etoh Fatty Liver
|
Etoh Fatty Liver Metamorphosis
|
Fatty Etoh Liver Necrosis
|
|
|
Eye Disease |
Eye Diseases
|
Abnormality Of The Eye
|
Toxoplasma Oculopathy
|
|
|
Telogen Effluvium |
|
|
Growth Hormone Secreting Pituitary Adenoma |
Somatotroph Adenoma
|
Growth Hormone-Secreting Pituitary Adenoma
|
Growth Hormone Producing Adenoma Of The Pituitary
|
Growth Hormone Secreting Adenoma Of Pituitary
|
|
|
Lymphoma |
Lymphoid Cancer
|
Lymphomas
|
Lymphoid Cancers
|
Lymphoid Neoplasm
|
Lymphoma Nos
|
Nhl - [Non-Hodgkin Lymphoma]
|
Non-Hodgkin Lymphoma
|
Non-Hodgkin Lymphoma, Nos
|
Non-Hodgkin Malignant Lymphoma Nos
|
|
|
Hypothyroidism, Congenital, Nongoitrous, 4 |
Tsh Deficiency
|
CHNG4
|
Thyrotropin Deficiency, Isolated
|
Pituitary Cretinism
|
Congenital Nongoitrous Hypothyroidism 4
|
Isolated Thyrotropin Deficiency
|
Thyroid-Stimulating Hormone Deficiency
|
Hypothyroidism, Congenital, Nongoitrous 4
|
Thyroid-Stimulating Hormone, Deficiency Of
|
Isolated Thyroid-Stimulating Hormone Deficiency
|
Isolated Tsh Deficiency
|
Hypothyroidism, Congenital, Nongoitrous, Type 4
|
Secondary Hypothyroidism
|
Tsh - [Thyroid Stimulating Hormone] Deficiency
|
|
|
Marasmus |
Nutritional Marasmus
|
Nutritional Atrophy
|
|
|
Cerebral Palsy |
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
Palsy Cerebral
|
Palsy, Cerebral
|
Cerebral Palsy, Mixed
|
|
|
Potter'S Syndrome |
Potter Sequence
|
Potter Syndrome
|
Oligohydramnios Sequence
|
Congenital Absence Of Kidneys Syndrome
|
|
|
Scoliosis |
|
|
Keratopathy |
|
|
Central Precocious Puberty |
Cpp
|
Gonadotropin-Dependant Precocious Puberty
|
Gonadotropin-Dependent Precocious Puberty
|
Precocious Puberty, Central
|
|
|
Androgenic Alopecia |
Androgenetic Alopecia
|
Alopecia Androgenetica, Male Pattern Baldness
|
|
|
Insulinoma |
Islet Cell Adenoma
|
Insulin-Producing Tumor Of Islet Cells
|
Adenoma Islet Cell
|
Islet Cell Tumor
|
Experimental Organism Islet Cell Adenoma Neoplasm
|
|
|
Retroperitoneal Hemangiopericytoma |
|
|
Adult Syndrome |
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
Acro Dermato Ungual Lacrimal Tooth Syndrome
|
Pigment Anomaly-Ectrodactyly-Hypodontia Syndrome
|
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
Adult
|
|
|
Hydrocephalus |
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
Tetanus |
Lockjaw
|
Clostridial Tetanus
|
Infection Due To Clostridium Tetani
|
Lock-Jaw
|
|
|
Colorectal Cancer |
Colon Cancer
|
Colorectal Carcinoma
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
Carcinoma Of Colon
|
CRC
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
Colorectal Carcinomas
|
Colon Cancers
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
Malignant Tumor Of Colon
|
|
|
Hypogonadotropic Hypogonadism |
Klinefelter Syndrome
|
Klinefelter'S Syndrome
|
Xxy Syndrome
|
Xxy Trisomy
|
Hypogonadotropism
|
47, Xxy
|
Congenital Idiopathic Hypogonadotropic Hypogonadism
|
Isolated Congenital Gonadotropin Deficiency
|
47,Xxy Syndrome
|
47, Xxy Syndrome
|
Klinefelters Syndrome
|
Hypogonadism
|
Klinefelter Syndrome In Males
|
Klinefelter Syndrome, Unspecified
|
Klinefelter Syndrome Karyotype 47, Xxy
|
|
|
Abetalipoproteinemia |
Acanthocytosis
|
ABL
|
Bassen-Kornzweig Syndrome
|
Mtp Deficiency
|
Familial Hypobetalipoproteinemia
|
Abetalipoproteinaemia
|
Microsomal Triglyceride Transfer Protein Deficiency
|
Microsomal Triglyceride Transfer Protein Deficiency Disease
|
Abetalipoproteinemia Neuropathy
|
Apolipoprotein B Deficiency
|
Bassen-Kornzweig Disease
|
Betalipoprotein Deficiency Disease
|
Congenital Betalipoprotein Deficiency Syndrome
|
Homozygous Familial Hypobetalipoproteinemia
|
Fhbl
|
Bassen Kornzweig Syndrome
|
Hypobetalipoproteinemia, Familial
|
Hypobetalipoproteinemia
|
Hypobetalipoproteinemias
|
Hypobetalipoproteinemia, Familial, Apolipoprotein B
|
|
|
Osteochondrosis |
Osteochondritis
|
Apophysitis
|
Epiphysitis
|
Osteochondritis Juvenilis
|
Epiphyseal Necrosis
|
Juvenile Osteochondrosis Of Tibial Tubercle
|
|
|
Heart Disease |
Heart Failure
|
Congenital Heart Disease
|
Heart Diseases
|
Congenital Heart Defects
|
Congenital Heart Defect
|
Heart Malformation
|
Congenital Anomaly Of Heart
|
Heart Defect
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
Heart Defects
|
Heart Disease, Congenital
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
Secondary Hypertrophic Osteoarthropathy |
Osteoarthropathy, Secondary Hypertrophic
|
Bamberger-Marie Disease
|
Hpoa - Hypertrophic Pulmonary Osteoarthropathy
|
Hypertrophic Pulmonary Osteoarthropathy
|
Marie Bamberger Disease
|
|
|
Uterine Benign Neoplasm |
|
|
Huntington Disease |
Huntington'S Disease
|
Huntington Chorea
|
Huntington'S Chorea
|
HD
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
Progressive Hereditary Chorea
|
|
|
Myopia |
Near-Sightedness
|
Short-Sightedness
|
Nearsightedness
|
Nearsighted
|
Near Vision
|
Close Sighted
|
Myopic
|
Short-Sighted
|
Near Sighted
|
|
|
Hypothalamic Disease |
Hypothalamic Diseases
|
Hypothalamic Dysfunction
|
Hypothalamic Disorder
|
Hypothalamic Dysfunction Syndromes
|
|
|
Reproductive Organ Benign Neoplasm |
|
|
Endocrine Organ Benign Neoplasm |
|
|
Vascular Disease |
Vascular Diseases
|
Aneurysm
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
Lung Disease |
Lung Diseases
|
Disorder Of Lung
|
Abnormality Of The Lung
|
|
|
Isolated Growth Hormone Deficiency |
Congenital Ighd
|
Congenital Isolated Gh Deficiency
|
Congenital Isolated Growth Hormone Deficiency
|
Non-Acquired Isolated Growth Hormone Deficiency
|
Pituitary Dwarfism
|
Dwarfism, Pituitary
|
Isolated Somatotropin Deficiency
|
Isolated Congenital Growth Hormone Deficiency
|
Familial Isolated Growth Hormone Deficiency
|
Ighd
|
Dwarfism, Growth Hormone Deficiency
|
Growth Hormone Deficiency Dwarfism
|
Isolated Gh Deficiency
|
Isolated Hgh Deficiency
|
Isolated Human Growth Hormone Deficiency
|
Isolated Somatotropin Deficiency Disorder
|
Dwarfism Pituitary
|
|
|
Pituitary Hypoplasia |
Hypoplasia Of The Pituitary Gland
|
|
|
Bone Remodeling Disease |
|
|
Bone Resorption Disease |
|
|
Thyroid Gland Disease |
Abnormality Of The Thyroid Gland
|
Thyroid Diseases
|
|
|
Prolactin Producing Pituitary Tumor |
Prolactin-Producing Pituitary Gland Carcinoma
|
Prolactin-Producing Pituitary Tumor
|
Malignant Prolactin Producing Neoplasm Of Pituitary Gland
|
Malignant Prolactinoma
|
Prolactin Producing Pituitary Tumour
|
Prolactin Secreting Tumor Of Pituitary
|
Prolactin Secreting Tumour Of Pituitary
|
|
|
Central Diabetes Insipidus |
Neurogenic Diabetes Insipidus
|
Diabetes Insipidus Cranial Type
|
Diabetes Insipidus Neurogenic
|
Diabetes Insipidus Neurohypophyseal
|
Neurohypophyseal Diabetes Insipidus
|
Pituitary Diabetes Insipidus
|
Cdi
|
Doid:0081055
|
Diabetes Insipidus
|
Di - [Diabetes Insipidus]
|
Adh - [Antidiuretic Hormone Secretion] Deficiency
|
Diabetes Mellitus Insipidus
|
Familial Diabetes Insipidus
|
Antidiuretic Hormone Hyposecretion
|
Vasopressin Deficiency Syndrome
|
Primary Central Diabetes Insipidus
|
Vasopressin Deficiency
|
Vasopressin Hyposecretion
|
Diabetes Insipidus Secondary To Vasopressin Deficiency
|
|
|
Pigmentation Disease |
Pigmentation Disorders
|
Skin Pigmentation Disorder
|
|
|
Aromatase Excess Syndrome |
AEXS
|
Increased Aromatase Activity
|
Familial Hyperestrogenism
|
Hereditary Prepubertal Gynecomastia
|
Aromatase Activity, Increased
|
Familial Gynecomastia Due To Increased Aromatase Activity
|
Hereditary Gynecomastia
|
Gynecomastia, Familial
|
Familial Gynecomastia
|
|
|
Isolated Growth Hormone Deficiency, Type Ii |
Ighd Ii
|
Isolated Growth Hormone Deficiency Type Ii
|
IGHD2
|
Growth Hormone Deficiency, Isolated, Type Ii
|
Congenital Ighd Type Ii
|
Congenital Isolated Gh Deficiency Type Ii
|
Congenital Isolated Growth Hormone Deficiency Type Ii
|
Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency Autosomal Dominant
|
Growth Hormone Deficiency, Isolated, Autosomal Dominant
|
Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency, Autosomal Dominant
|
Autosomal Dominant Isolated Growth Hormone Deficiency
|
Autosomal Dominant Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency
|
Isolated Growth Hormone Deficiency Type 2
|
Growth Hormone Deficiency, Isolated Autosomal Dominant
|
Growth Hormone Deficiency, Isolated, 2
|
Growth Hormone Deficiency Isolated Autosomal Dominant
|
|
|
Glioblastoma |
Glioblastoma Multiforme
|
Gbm
|
Adult Glioblastoma Multiforme
|
Grade Iv Adult Astrocytic Tumor
|
Primary Glioblastoma Multiforme
|
Spongioblastoma Multiforme
|
Adult Glioblastoma
|
Primary Glioblastoma
|
|
|
Rhabdomyosarcoma |
|
|
Apnea, Obstructive Sleep |
Obstructive Sleep Apnea Syndrome
|
Obstructive Sleep Apnea
|
Sleep Apnea, Obstructive
|
Osa
|
Osas
|
Sleep Apnea/Hypopnea Syndrome
|
Sahs
|
Upper Airway Resistance Sleep Apnea Syndrome
|
Apnea, Obstructive
|
Obstructive Apnea
|
Osahs
|
Sleep Apnea Hypopnea Syndrome
|
Sleep Apnea Syndrome, Obstructive
|
Sleep Apnea Obstructive
|
Sleep Apnea Syndromes
|
Obstructive Sleep Apnoea Syndrome
|
Obstructive Sleep Apnoea, Adult
|
Osa - [Obstructive Sleep Apnoea]
|
Obstructive Sleep Apnoea, Paediatric
|
Obstructive Sleep Apnoea Hypopnoea Syndrome
|
Osa Syndrome
|
Sleep Apnoea Nos
|
[Sas] - Sleep Apnoea Syndrome
|
Sleep Apnoea Syndrome
|
[Osahs] - Obstructive Sleep Apnoea-Hypopnea Syndrome
|
[Sahs] - Sleep Apnoea-Hypopnea Syndrome
|
|
|
Amyotrophic Lateral Sclerosis 1 |
Amyotrophic Lateral Sclerosis
|
ALS
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
Charcot Disease
|
ALS1
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
Lou Gehrig'S Disease
|
Mnd
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
Progressive Atrophic Paralysis
|
|
|
Lymphoid Interstitial Pneumonia |
Lymphocytic Interstitial Pneumonia
|
Lip Disease
|
Lip Diseases
|
LIP
|
Disease Of Lips
|
|
|
Islet Cell Tumor |
Pancreatic Neuroendocrine Tumor
|
Neuroendocrine Tumor Of Pancreas
|
Pnet
|
Pancreatic Net
|
Pancreatic Endocrine Tumor
|
Well-Differentiated Nen Of Pancreas
|
Well-Differentiated Neuroendocrine Neoplasm Of Pancreas
|
Well-Differentiated Pancreatic Nen
|
Well-Differentiated Pancreatic Neuroendocrine Neoplasm
|
Endocrine Pancreas Cancer
|
Islet Cell Neoplasm
|
Islet Cell Tumour
|
Malignant Pancreatic Endocrine Tumor
|
Malignant Pancreatic Endocrine Tumour
|
Malignant Tumor Of Endocrine Pancreas
|
Malignant Tumour Of Endocrine Pancreas
|
Pancreatic Endocrine Neoplasm
|
Pancreatic Neuroendocrine Neoplasm
|
Adenoma, Islet Cell
|
Well Differentiated Pancreatic Endocrine Tumor
|
Malignant Neoplasm Of Endocrine Pancreas
|
Pancreatic Endocrine Carcinoma
|
|
|
Kwashiorkor |
Kwashiokor
|
Nutritional Edema With Dyspigmentation Of Skin And Hair
|
Nutritional Oedema With Dyspigmentation Of Skin And/Or Hair
|
|
|
Intracranial Hypertension, Idiopathic |
Pseudotumor Cerebri
|
Idiopathic Intracranial Hypertension
|
Benign Intracranial Hypertension
|
Iih
|
Benign Intracran. Hypt.
|
|
|
Pre-Eclampsia |
Preeclampsia
|
Gestational Hypertension
|
Hypertension Induced By Pregnancy
|
Pre-Eclamptic Toxaemia
|
Pregnancy Associated Hypertension
|
Proteinuric Hypertension Of Pregnancy
|
Hypertension, Pregnancy-Induced, Susceptibility To
|
Preeclampsia/Eclampsia
|
Pregnancy Toxemia
|
Toxaemia Of Pregnancy
|
Gestational Proteinuric Hypertension
|
Pregnancy-Induced Hypertension
|
Toxemia Of Pregnancy
|
Preeclampsia, Susceptibility To
|
Transient Hypertension Of Pregnancy
|
Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria
|
Gestational Hypertension Nos
|
Mild Proteinuric Hypertension Of Pregnancy
|
Pih - [Pregnancy-Induced Hypertension]
|
Pregnancy-Induced Hypertension Nos
|
Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria
|
Pe - [Pre-Eclampsia]
|
Pre-Eclampsia Nos
|
Pre-Eclamptic Nos
|
Pregnancy Pre-Eclampsia
|
Puerperal Pre-Eclampsia
|
Pre-Eclampsia Toxaemia
|
Toxaemia In Pregnancy
|
Pet - [Pre-Eclamptic Toxaemia]
|
Maternal Toxaemia
|
|
|
Adenoid Hypertrophy |
Hypertrophy Of Adenoids
|
Adenoidal Hypertrophy
|
Enlarged Adenoids
|
Enlargement Of Adenoids
|
Adenoidal Enlargement
|
Adenoids, Hypertrophy
|
Hypertrophy Of Adenoids Alone
|
Adenoid Growth
|
Hyperplasia Of Adenoids
|
Hypertrophy Of Pharyngeal Tonsil
|
|
|
Amelogenesis Imperfecta, Type Ig |
Enamel-Renal Syndrome
|
Ers
|
Amelogenesis Imperfecta Type 1g
|
AI1G
|
Enamel-Renal-Gingival Syndrome
|
Amelogenesis Imperfecta And Gingival Fibromatosis Syndrome
|
Aigfs
|
Amelogenesis Imperfecta, Hypoplastic, With Nephrocalcinosis
|
Amelogenesis Imperfecta Hypoplastic With Nephrocalcinosis
|
Amelogenesis Imperfecta Type Ig
|
Amelogenesis Imperfecta-Nephrocalcinosis Syndrome
|
Amelogenesis Imperfecta 1g
|
Hypoplastic Amelogenesis Imperfecta With Nephrocalcinosis
|
Amelogenesis Imperfecta Nephrocalcinosis
|
|
|
Persistent Fetal Circulation Syndrome |
Persistent Fetal Circulation
|
Fetal Circulation
|
Persistent Pulmonary Hypertension Of The Newborn
|
Congenital Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
|
Persistent Foetal Circulation
|
Persistent Foetal Circulation Syndrome
|
Pfc - [Persistent Fetal Circulation] Syndrome
|
Pphn - [Persistent Pulmonary Hypertension Of The Newborn]
|
Newborn Pulmonary Hypertension
|
Primary Pulmonary Hypertension Of Newborn
|
|
|
Functionless Pituitary Adenoma |
Non-Functioning Neoplasm Of The Pituitary
|
Non-Secretory Adenoma Of The Pituitary Gland
|
Non-Functioning Pituitary Gland Neoplasm
|
|
|
Glucocorticoid-Induced Osteoporosis |
Steroid-Induced Osteoporosis
|
|
|
Osteogenic Sarcoma |
Osteosarcoma
|
OSRC
|
Osteosarcoma, Somatic
|
Neoplasms, Bone Tissue
|
Bone Tissue Neoplasm
|
Osteoid Sarcoma
|
Skeletal Sarcoma
|
Osteosarcoma Of Bone
|
Bone Sarcoma
|
|
|
Three M Syndrome 1 |
3-M Syndrome
|
Yakut Short Stature Syndrome
|
3m Syndrome
|
Le Merrer Syndrome
|
Dolichospondylic Dysplasia
|
Gloomy Face Syndrome
|
Three M Syndrome
|
3M1
|
3m Syndrome 1
|
Miller-Mckusick-Malvaux Syndrome
|
3-Msbn
|
Three-M Slender-Boned Nanism
|
Miller-Mckusick-Malvaux-Syndrome
|
3-M Syndrome 1
|
3m Syndrome-1
|
3m Syndrome, Type 1
|
Dwarfism
|
Dwarfism Tall Vertebrae
|
|
|
Adrenal Gland Disease |
Adrenal Gland Diseases
|
Adrenal Gland Disorders
|
|
|
Parathyroid Gland Disease |
Parathyroid Diseases
|
Disease Of Parathyroid Glands
|
Parathyroid Disease
|
|
|
Decubitus Ulcer |
Pressure Ulcer
|
Pressure Sores
|
Pressure Ulcers
|
Bedsore
|
Decubitus Ulcer
|
Decubitus Ulcer Any Site
|
|
|
Muscular Dystrophy |
Muscular Dystrophies
|
Congenital Md
|
Congenital Muscular Dystrophy
|
Cmd
|
Mdc
|
Dystrophy, Muscular
|
Gower'S Muscular Dystrophy
|
Progressive Musclular Dystrophy
|
Pseudohypertrophic Atrophy
|
Pseudohypertrophic Muscle Paralysis
|
Pseudohypertrophic Muscular Atrophy
|
Pseudohypertrophic Muscular Dystrophy
|
Pseudohypertrophic Paralysis
|
Pseudomuscular Hypertrophy
|
|
|
Acquired Metabolic Disease |
|
|
Autism Spectrum Disorder |
Asd
|
Autism Spectrum Disorders
|
Autistic Continuum
|
Pervasive Developmental Disorder
|
Pervasive Development Disorder
|
Autistic Behavior
|
Autistic Disorder
|
Autistic
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
Childhood Autism
|
Kanner Syndrome
|
Pervasive Developmental Delay Nos
|
Pervasive Developmental Disorder, Not Otherwise Specified
|
|
|
Anxiety |
Anxiety Disorder
|
Anxiety Disorders
|
Anxiety State
|
Anxieties
|
Anxiety Neurosis
|
|
|
Myocardial Infarction |
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
Myocardial Infarct
|
MCI1
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
Pheochromocytoma |
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
PCC
|
Chromaffin Cell Tumor
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
Pheochromoblastoma
|
Pheochromocytomas
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
Exophthalmos |
|
|
Premature Menopause |
Primary Ovarian Insufficiency
|
Premature Ovarian Failure
|
Hypergonadotropic Hypogonadism
|
Premature Ovarian Insufficiency
|
Menopause - Premature
|
Menopause Praecox
|
Menopause Premature
|
Menopause, Premature
|
Female Hypergonadotropic Hypogonadism
|
Hypergonadotrophic Ovarian Failure
|
Primary Female Hypogonadism
|
Pof - [Premature Ovarian Failure]
|
Ovarian Failure
|
Ovarian Secretion Suppression
|
Ovary Hyposecretion
|
Ovary Secretion Deficiency
|
Premature Menopause Nos
|
|
|
Overnutrition |
|
|
Eating Disorder |
Eating Disorders
|
Feeding And Eating Disorders
|
|
|
Autoimmune Disease Of Endocrine System |
|
|
Postpoliomyelitis Syndrome |
Postpolio Syndrome
|
Post-Polio Syndrome
|
Post Polio Syndrome
|
Polio Late Effects
|
Post-Polio Muscular Atrophy
|
Post-Polio Sequelae
|
Post-Poliomyelitic Syndrome
|
Postpolio Sequelae
|
Postpoliomyelitic Syndrome
|
Postpoliomyelitis Sequelae
|
|
|
Glucose Metabolism Disease |
Glucose Metabolism Disorders
|
Disorder Of Glucose Metabolism
|
|
|
Carbohydrate Metabolic Disorder |
Inborn Errors Of Carbohydrate Metabolism
|
Disorder Of Carbohydrate Metabolism
|
Carbohydrate Metabolism, Inborn Errors
|
Disorder Of Carbohydrate Transport And Metabolism
|
Inborn Carbohydrate Metabolism Disorder
|
Inborn Carbohydrate Metabolic Disorder
|
Carbohydrate Metabolism Disorder
|
Carbohydrate Metabolism Disorders
|
Disorders Of Carbohydrate Metabolism
|
Congenital Disorders Of Carbohydrate Metabolism
|
Inherited Disorders Of Carbohydrate Metabolism
|
|
|
Acromesomelic Dysplasia 1 |
Acromesomelic Dysplasia, Maroteaux Type
|
Amdm
|
Acromesomelic Dysplasia 1, Maroteaux Type
|
AMD1
|
St. Helena Dysplasia
|
Acromesomelic Dysplasia-1
|
Acromesomelic Dysplasia Maroteaux Type
|
Acromesomelic Dwarfism Maroteux Type
|
Dysplasia, Acromesomelic, Type 1, Maroteaux
|
Acromesomelic Dysplasia Hunter-Thompson Type
|
|
|
Diabetic Polyneuropathy |
Diabetes Mellitus With Polyneuropathy
|
Polyneuropathy In Diabetes
|
Diabetic Polyneuropathies
|
Diabetic Neuropathy Nos
|
|
|
Disorder Of Sexual Development |
Disorder Of Sex Development
|
Disorders Of Sex Development
|
Sex Development Disorder
|
Sex Differentiation Disease
|
Dsd
|
Sex Differentiation Disorders
|
|
|
Cataract |
Cataracts
|
Cat - [Cataract]
|
Cataract Form
|
Lens Opacity
|
Lens Opacities
|
|
|
Ulcer Of Lower Limbs |
Ulcer Of Ankle
|
Ulcer Of Calf
|
Ulcer Of Heel And Midfoot
|
Ulcer Of Thigh
|
Ulcer Of Lower Limb
|
|
|
Body Dysmorphic Disorder |
Dysmorphophobia
|
Body Dysmorphia
|
Dysmorphic Syndrome
|
Body Dysmorphic Disorders
|
|
|
Skin Atrophy |
Atrophic Condition Of Skin
|
Atrophoderma
|
Atrophy - Skin
|
|
|
Chronic Ulcer Of Skin |
Chronic Wounds
|
Callous Ulcer
|
Indolent Ulcer
|
Chronic Ulcer
|
|
|
Tendinitis |
|
|
Deficiency Anemia |
Anemia
|
Deficiency Anemias
|
Anaemia
|
|
|
Lissencephaly, X-Linked, 2 |
X-Linked Lissencephaly With Abnormal Genitalia
|
Hydranencephaly With Abnormal Genitalia
|
Xlag
|
Xlisg
|
X-Linked Lissencephaly With Ambiguous Genitalia
|
LISX2
|
Lissencephaly, X-Linked 2
|
X-Linked Lissencephaly 2
|
X-Linked Lissencephaly-Corpus Callosum Agenesis-Genital Anomalies Syndrome
|
Xlag Syndrome
|
Lissencephaly, X-Linked, With Ambiguous Genitalia
|
Xlis2
|
X-Linked Lissencephaly - Agenesis Of The Corpus Callosum - Genital Anomalies
|
X-Linked Lissencephaly-Agenesis Of The Corpus Callosum-Genital Anomalies Syndrome
|
Xlag Syndrome
|
Lissencephaly X-Linked With Ambiguous Genitalia
|
Lissencephaly, X-Linked, Type 2
|
Chromosome Xq26.3 Duplication Syndrome
|
|
|
Neuroblastoma |
Nb
|
Neuroblastoma, Susceptibility To
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
Hypertension, Essential |
Essential Hypertension
|
Hypertension
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
Hypertensive Disease
|
Primary Hypertension
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
Hyperpiesia
|
Idiopathic Hypertension
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
Htn
|
Vascular Hypertensive Disorder
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
Arterial Hypertension Nos
|
Hypertension Nos
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
Systemic Hypertension
|
Artery Htn
|
Benign Htn
|
Vascular Htn
|
Vascular Hypertension
|
Cholesterol Hypertension
|
Cholesterol Htn
|
Idiopathic Htn
|
Malignant Hypertension
|
Malignant Htn
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
Hypertensive Vascular Degeneration
|
|
|
Myopathy |
Muscular Diseases
|
Myopathies
|
|
|
Sleep Disorder |
Sleep Disorders
|
Non-Organic Sleep Disorder
|
|
|
Prostatic Hypertrophy |
Benign Prostatic Hypertrophy
|
Prostatic Hyperplasia
|
|
|
Myeloma, Multiple |
Multiple Myeloma
|
Plasma Cell Myeloma
|
Kahler Disease
|
Myelomatosis
|
Medullary Plasmacytoma
|
Multiple Myeloma, Resistance To
|
Myeloma
|
Plasma Cell Dyscrasia
|
Kahler'S Disease
|
Multiple Myeloma, Susceptibility To
|
Myeloma - Multiple
|
Kahler-Bozzolo Disease
|
Plasma Cell Myelomas
|
MM
|
Plasma Cell Neoplasm
|
Primary Systemic Amyloidosis
|
Primary Amyloidosis
|
Immunoglobulin Deposition Disease
|
Plasmacytic Myeloma
|
Multiple Myelomata
|
Multiple Myeloma Nos
|
Multiple Myeloma Without Mention Of Remission
|
Monostotic Plasma Cell Myeloma
|
Mm - [Multiple Myeloma]
|
|
|
Carney Complex Variant |
Carney Complex
|
Carney Syndrome
|
Carney Complex, Type 1
|
Lamb Syndrome
|
Name Syndrome
|
Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome
|
Carney Complex - Trismus - Pseudocamptodactyly Syndrome
|
Carney Complex, Type 2
|
Car
|
Cnc1
|
Carney Myxoma-Endocrine Complex
|
Myxoma - Spotty Pigmentation - Endocrine Overactivity
|
Myxoma, Spotty Pigmentation, And Endocrine Overactivity
|
Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
|
Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
|
Carney Complex-Trismus-Pseudocamptodactyly Syndrome
|
CACOV
|
|
|
Lung Cancer |
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
Lung Cancer, Susceptibility To
|
Lung Cancer, Protection Against
|
Adenocarcinoma Of Lung, Somatic
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer
|
Lung Neoplasm
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
Non-Small Cell Lung Cancer
|
Nsclc
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
Cancer Of Lung
|
Cancer Of Bronchus
|
Cancer Of The Lung
|
Lung Malignancies
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
Respiratory Carcinoma
|
LNCR
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
Lung Carcinomas
|
Cancer, Lung
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
Bronchioloalveolar Adenocarcinoma
|
|
|
Bone Structure Disease |
|
|
Pancreatic Cancer |
Pancreatic Carcinoma
|
Carcinoma Of Pancreas
|
Familial Pancreatic Carcinoma
|
Pancreatic Neoplasm
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
Familial Pancreatic Cancer
|
Neoplasm Of The Pancreas
|
Cancer Of The Pancreas
|
Pancreatic Carcinoma, Somatic
|
Pancreatic Cancer, Somatic
|
Ca Body Of Pancreas
|
Ca Head Of Pancreas
|
Ca Tail Of Pancreas
|
Malignant Neoplasm Of Body Of Pancreas
|
Malignant Neoplasm Of Head Of Pancreas
|
Malignant Neoplasm Of Tail Of Pancreas
|
Pancreas Neoplasm
|
Exocrine Cancer
|
Exocrine Pancreas Carcinoma
|
Hereditary Pancreatic Cancer
|
Hereditary Pancreatic Carcinoma
|
PNCA
|
Pancreatic Cancer, Susceptibility To
|
Carcinoma Of Head Of Pancreas
|
Pancreatic Neoplasms
|
Pancreatic Tumors
|
Cancer, Pancreatic
|
Cancer Of Pancreas
|
Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site
|
|
|
Estrogen-Receptor Positive Breast Cancer |
|
|
Inherited Metabolic Disorder |
Inborn Errors Of Metabolism
|
Inborn Metabolic Disorder
|
Inborn Metabolism Disorder
|
Metabolic Hereditary Disorder
|
Inborn Error Of Metabolism
|
Metabolism, Inborn Errors
|
|
|
Teeth Hard Tissue Disease |
|
|
Cystic Fibrosis |
Mucoviscidosis
|
CF
|
Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis
|
Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis
|
Cystic Fibrosis Lung Disease, Modifier Of
|
Cystic Fibrosis Of Pancreas
|
Fibrocystic Disease Of Pancreas
|
Cf - [Cystic Fibrosis]
|
Cystic Fibrosis Nos
|
Fibrocystic Disease
|
Fibrocystic Disease Of The Pancreas
|
Mucoviscidosis Of Pancreas
|
Nonproliferative Fibrocystic Disease
|
Pancreatic Cystic Fibrosis
|
|
|
Fetal Alcohol Syndrome |
Fetal Alcohol Spectrum Disorders
|
Arbd
|
Arnd
|
Alcohol-Related Birth Defects
|
Alcohol-Related Neurodevelopmental Disorder
|
Fas
|
Fasd
|
Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta Or Breast Milk
|
Alcohol Related Birth Defect
|
Alcohol Related Neurodevelopmental Disorder
|
Alcohol Affecting Fetus Or Newborn Via Placenta Or Breast Milk
|
Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta And/Or Breast Milk
|
Dysmorphism Due To Alcohol
|
Fetal Etoh Syndrome
|
|
|
Cell Type Benign Neoplasm |
|
|
Macular Degeneration, Age-Related, 1 |
Macular Degeneration
|
Age-Related Macular Degeneration
|
Macular Degeneration, Age-Related
|
Age Related Macular Degeneration
|
Age Related Macular Degeneration 1
|
ARMD1
|
Senile Macular Degeneration
|
Maculopathy, Age-Related, 1
|
Macular Degeneration, Age-Related, Reduced Risk Of
|
Age Related Maculopathy 1
|
Age Related Maculopathies
|
Age Related Maculopathy
|
Senile Macular Retinal Degeneration
|
Macular Degeneration Of Retina
|
Age-Related Maculopathy
|
Amd
|
Armd
|
Age-Related Maculopathy, Susceptibility To
|
Maculopathy Age-Related
|
Macular Degeneration, Age-Related, 1, Susceptibility To
|
Maculopathy, Age-Related
|
Macular Degeneration, Age-Related, Type 1
|
Macular Degeneration, Age-Related, 2
|
|
|
Bipolar Disorder |
Bipolar Depression
|
Manic Disorder
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
Manic Bipolar I Disorder
|
Manic Depression
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
Major Affective Disorder
|
Major Affective Disorder 1
|
Major Affective Disorder 2
|
|
|
Muscle Tissue Disease |
|
|
Malaria |
Malaria, Susceptibility To
|
Malaria, Resistance To
|
Malaria, Cerebral
|
Cerebral Malaria
|
Malaria, Severe, Susceptibility To
|
Malaria, Severe, Resistance To
|
Malaria, Cerebral, Susceptibility To
|
Induced Malaria
|
Malaria, Vivax, Protection Against
|
Malaria, Severe
|
Malaria, Cerebral, Reduced Risk Of
|
Malaria, Protection Against
|
Resistance To Malaria Due To G6pd Deficiency
|
Malaria Due To G6pd Deficiency
|
Malarial Encephalitis
|
CM
|
Malaria Cerebral
|
Susceptibility To Malaria
|
Acute Pernicious Fever
|
Aestivo-Autumnal Fever
|
Aestivo Autumnal Malaria
|
Chagres Fever
|
Continued Malaria Fever
|
Estivo-Autumnal Fever
|
Estivo-Autumnal Malaria
|
Estivo-Autumnal Malarial Fever
|
Falciparum Fever
|
Malignant Tertian Fever
|
Malignant Tertian Malaria
|
Pernicious Intermittent Fever
|
Pernicious Malaria
|
Quotidian Malaria
|
Subtertian Fever
|
Subtertian Malaria Fever
|
Subtertian Malignant Tertian Malaria
|
Tropical Malaria
|
Algid Malaria
|
Bilious Haemoglobinuric Fever
|
Black Water Fever
|
Blackwater Fever
|
Malarial Blackwater Fever
|
Severe Malarial Falciparum
|
West African Fever
|
Malarial Haematinuria
|
Haemoglobinuric Fever
|
Haemoglobinuric Malaria
|
Severe Plasmodium Falciparum Malaria
|
Malarial Haemoglobinuria
|
Malarial Haematuria
|
Falciparum Malaria [Malignant Tertian]
|
Malaria Tropica
|
Malarial Shock
|
Chagres Virus Disease
|
Malignant Malaria
|
Mtm - [Malignant Tertian Malaria]
|
Tm -[Malignant Tertian Malaria]
|
Panama Fever
|
St - [Subtertian Malaria]
|
Malarial Quotidian
|
Benign Tertian Malaria
|
Tertian Ague
|
Vivax Fever
|
Plasmodium Vivax Malaria Nos
|
Btm - [Benign Tertian Malaria]
|
Bt - [Benign Tertian Malaria]
|
Vivax Malaria
|
Benign Tertian Vivax Malaria
|
Tertian Malaria
|
Quartan Malaria
|
Quartan Ague
|
Quartan Fever
|
Plasmodium Malariae Malaria Nos
|
Quartan Malarial
|
Malaria By Plasmodium Malariae
|
Malariae Malaria
|
Ovale Tertian Malaria
|
Plasmodium Ovale Fever
|
Malaria Fever By Plasmodium Ovale
|
Ovale Malaria
|
Malaria By Plasmodium Ovale
|
Malarial Ovale
|
Marsh Fever
|
Remittent Congestive Fever
|
Coastal Fever
|
Remittent Gastric Fever
|
Miasmatic Fever
|
Congestive Remittent Fever
|
Intermittent Fever
|
Jungle Fever
|
Paludism
|
Cameroon Fever
|
Ague
|
Corsican Fever
|
Intermittent Bilious Fever
|
Disease Due To Plasmodiidae
|
Malarial Fever
|
Plasmodiosis
|
Remittent Fever
|
Roman Fever
|
Malaria Fever Nos
|
Malaria Nos
|
Paludal Fever
|
Clinically Diagnosed Malaria
|
Clinically Diagnosed Malaria Without Parasitological Confirmation
|
Congestive Fever
|
Malarial Cachexia
|
Marsh Cachexia
|
Paludal Cachexia
|
Recurrent Malaria
|
Remittent Malaria
|
|
|
Muscular Disease |
|
|
Colorectal Adenoma |
Colorectal Adenomas
|
Adenoma Of Large Intestine
|
|
|
Hair Disease |
Hair Diseases
|
Hair Anomaly
|
Hair Disorder
|
Hair Problems
|
|
|
Autism |
Autistic Disorder
|
Autism Susceptibility 1
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
Kanner'S Syndrome
|
Autistic
|
|
|
Septooptic Dysplasia |
Septo-Optic Dysplasia
|
De Morsier Syndrome
|
Growth Hormone Deficiency With Pituitary Anomalies
|
SOD
|
Pituitary Hormone Deficiency, Combined, 5
|
Septo-Optic Dysplasia Spectrum
|
Septo-Optic Dysplasia With Growth Hormone Deficiency
|
Pituitary Hormone Deficiency, Combined 5
|
Hypopituitarism And Septooptic 'Dysplasia'
|
GHDPA
|
CPHD5
|
Dysplasia, Septo-Optic
|
Kallmann Syndrome
|
|
|
Fetal Alcohol Spectrum Disorder |
Fetal Alcohol Spectrum Disorders
|
Fetal Alcohol Syndrome
|
|
|
Inflammatory Bowel Disease |
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
Silver-Russell Syndrome 1 |
Silver-Russell Syndrome
|
Russell-Silver Syndrome
|
Silver-Russell Dwarfism
|
Rss
|
SRS1
|
Srs
|
Silver Russell Dwarfism
|
Russell Silver Syndrome
|
Silver Russell Syndrome
|
|
|
Rasopathy |
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
Ovarian Cancer |
Ovarian Carcinoma
|
Ovarian Neoplasm
|
Malignant Tumour Of Ovary
|
Cancer Of The Ovary
|
Epithelial Ovarian Cancer
|
Neoplasm Of Ovary
|
Ovarian Neoplasms
|
Ovarian Cancers
|
Malignant Neoplasm Of Ovary
|
Primary Malignant Neoplasm Of Ovary
|
Ovarian Cancer, Somatic
|
Malignant Ovarian Tumor
|
Ovary Neoplasm
|
Primary Ovarian Cancer
|
Tumor Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
OC
|
Ovarian Carcinomas
|
Cancer, Ovarian
|
Cancer Of Ovary
|
Ovary Cancer
|
Ca Ovary
|
|
|
Asbestos-Related Lung Carcinoma |
|
|
Soft Palate Cancer |
Malignant Tumor Of Soft Palate
|
Malignant Tumor Of The Soft Palate
|
Palate Cancer Soft Palate
|
|
|
Specific Developmental Disorder |
|
|
Lipoid Congenital Adrenal Hyperplasia |
Congenital Adrenal Hyperplasia
|
Congenital Lipoid Adrenal Hyperplasia Due To Star Deficency
|
Congenital Lipoid Adrenal Hyperplasia
|
Lipoid Cah
|
Lipoid Adrenal Hyperplasia
|
Adrenal Hyperplasia 1
|
Cah
|
Clah
|
LCAH
|
Adrenal Hyperplasia I
|
Lipoid Hyperplasia, Congenital, Of Adrenal Cortex With Male Pseudohermaphroditism
|
Congenital Adrenal Hyperplasia Lipoid
|
Adrenal Hyperplasia, Congenital
|
Congenital Adrenal Hyperplasia, Lipoid
|
AH1
|
Congenital Lipoid Hyperplasia Of Adrenal Cortex With Male Pseudohermaphroditism
|
Adrenal Hyperplasia Congenital
|
Hyperplasia, Adrenal, Lipoid, Congenital
|
Congenital Adrenogenital Disorders Associated With Enzyme Deficiency
|
Congenital Adrenal Cortical Hyperplasia
|
Congenital Adrenal Gland Hyperplasia
|
Congenital Adrenogenital Syndrome
|
Congenital Hyperadrenocorticism
|
Congenital Adrenogenitalism
|
Congenital Female Adrenal Pseudohermaphroditism
|
|
|
Gastrointestinal System Benign Neoplasm |
|
|
Gastric Cancer |
Stomach Cancer
|
Gastric Carcinoma
|
Stomach Carcinoma
|
Gastric Cancer, Somatic
|
Gastric Neoplasm
|
Carcinoma Of Stomach
|
Stomach Neoplasms
|
Malignant Neoplasm Of Stomach
|
Gastric Cancer Risk After H. Pylori Infection
|
Cancer Of The Stomach
|
Adult Stomach Cancer
|
Adult Stomach Carcinoma
|
GASC
|
Gastric Cancer Intestinal
|
Gastric Cancers
|
Gastric Carcinomas
|
Cancer, Gastric
|
Stomach Neoplasm
|
Malignant Neoplasm Of Body Of Stomach
|
Malignant Tumor Of Lesser Curve Of Stomach
|
Gastrocarcinoma Of Unspecified Site
|
Leather Bottle Stomach
|
Carcinoma Of Fundus Of Stomach
|
Cancer Of Fundus Of Stomach
|
Primary Malignant Neoplasm Of Body Of Stomach
|
Cancer Of Body Of Stomach
|
Primary Malignant Neoplasm Of Pyloric Antrum
|
Pyloric Antrum Cancer
|
Malignant Tumour Of Stomach
|
|
|
Chromosomal Disease |
Chromosomal Disorders
|
Congenital Chromosomal Disease
|
|
|
Beta-Thalassemia Major |
Cooley'S Anemia
|
Cooley Anemia
|
Mediterranean Anemia
|
|
|
Atrial Septal Defect 8 |
ASD8
|
Atrial Heart Septal Defect 8
|
Septal Defect, Atrial, Type 8
|
|
|
Amelogenesis Imperfecta |
Ai
|
Congenital Enamel Hypoplasia
|
Al - [Amelogenesis Imperfecta]
|
|
|
Lipid Metabolism Disorder |
Dyslipidemia
|
Disorder Of Fatty Acid Metabolism
|
Lipid Metabolism Disorders
|
Fatty Acid Metabolism Disorder
|
Disorder Of Lipid Metabolism
|
Abnormality Of Lipid Metabolism
|
Lipid Metabolism, Inborn Errors
|
Dyslipidemias
|
Disorders Of Lipid Metabolism
|
Congenital Disorders Of Lipid Metabolism
|
Inherited Disorders Of Lipid Metabolism
|
|
|
Peripheral Nervous System Disease |
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
Cryptorchidism, Unilateral Or Bilateral |
Cryptorchidism
|
Undescended Testicle
|
Undescended Testis
|
Cryptorchism
|
Undescended Testicles
|
CRYPTO
|
Impaired Testicular Descent
|
Cryptosporidiosis
|
Retained Testis
|
Unilateral Cryptorchidism
|
Unilateral Undescended Testis
|
Nondescent Unilateral Testicle
|
Unilateral Cryptorchism
|
Ectopic Testis, Unilateral
|
Bilateral Cryptorchidism
|
Bilateral Cryptorchism
|
Bilateral Nondescent Testicle
|
Bilateral Undescended Testes
|
Bilateral Ectopic Testes
|
|
|
Osteochondrodysplasia |
Skeletal Dysplasia
|
Chondrodystrophy
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
Schizophrenia |
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
Schizophrenia-1
|
Dementia Praecox
|
Schizophrenia 1
|
|
|
Patent Ductus Arteriosus 1 |
Patent Ductus Arteriosus
|
PDA1
|
Pda
|
Ductus Arteriosus, Patent
|
Patent Ductus Arteriosus, Susceptibility To
|
Patent Ductus Botalli
|
Patency Of The Ductus Arteriosus
|
Patent Ductus Arteriosus Familial
|
Ductus Arteriosus Patent
|
Patent Ductus Arteriosus - Persisting Type
|
|
|
Breast Adenocarcinoma |
Mammary Adenocarcinoma
|
Adenocarcinoma Of Breast
|
|
|
Brittle Bone Disorder |
Osteogenesis Imperfecta
|
Brittle Bone Disease
|
Fragilitas Ossium
|
Osteopsathyrosis
|
Lobstein Disease
|
Oi
|
Vrolik Disease
|
Lobstein'S Disease
|
Lobstein'S Syndrome
|
Vrolik'S Disease
|
Porak And Durante Disease
|
Glass Bone Disease
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
Osteogenesis Imperfecta, Recessive Perinatal Lethal
|
Brittle Bone Syndrome
|
Oi - [Osteogenesis Imperfecta]
|
Ossium Fragility
|
Osteitis Fragilitans
|
Bony Fragility
|
Blue Sclera With Fragility Of Bone And Deafness
|
White Blue Sclera - Fragility Of Bone - Deafness
|
|
|
Colonic Benign Neoplasm |
Colon Neoplasm
|
Colonic Mass
|
Colonic Tumor
|
Neoplasm Of Colon
|
Neoplasm Of The Colon
|
Colonic Neoplasms
|
Colon Cancer
|
Colon Carcinoma Nos
|
Colonic Cancer
|
Metastatic Colon Cancer Nos
|
|
|
Celiac Disease 1 |
Celiac Disease
|
Coeliac Disease
|
Celiac Sprue
|
Celiac Disease, Susceptibility To
|
Gluten-Sensitive Enteropathy
|
Nontropical Sprue
|
Sprue
|
CELIAC1
|
Celiac Disease, Susceptibility To, 1
|
Celiac Sprue 1
|
Celiac Sprue, Susceptibility To, 1
|
Gluten-Sensitive Enteropathy 1
|
Gluten-Sensitive Enteropathy, Susceptibility To, 1
|
Idiopathic Steatorrhea
|
Cœliac Disease
|
Gluten Intolerance
|
Gluten-Induced Enteropathy
|
Gluten Enteropathy
|
Celiac Disease, Susceptibility To, Type 1
|
Childhood Celiac Disease
|
Coeliac Rickets
|
Gee Disease
|
Gee-Herter Disease
|
Heubner-Herter Disease
|
Idiopathic Steatorrhoea
|
Thaysen'S Disease
|
Herter Gee Syndrome
|
|
|
Beckwith-Wiedemann Syndrome |
Wiedemann-Beckwith Syndrome
|
BWS
|
Exomphalos-Macroglossia-Gigantism Syndrome
|
Emg Syndrome
|
Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation
|
Emg Abnormality
|
Wbs
|
Exomphalos Macroglossia Gigantism Syndrome
|
Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation
|
Macroglossia Exomphalos Gigantism
|
|
|
Connective Tissue Disease |
Connective Tissue Diseases
|
Connective Tissue Disorder
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
Connective Tissue Disorders
|
|
|
Nervous System Disease |
Abnormality Of The Nervous System
|
Nervous System Diseases
|
Nervous System Disorder
|
|
|
Meningioma, Familial |
Meningioma
|
Familial Meningioma
|
Meningioma, Familial, Susceptibility To
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Meningeal Neoplasm
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Meningeal Neoplasms
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Meningiomas
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Meningioma, Nf2-Related, Somatic
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Meningioma, Sis-Related
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Meningothelial Cell Tumor
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Neoplasm Of The Meninges
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Primary Meningeal Tumor
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Familial Multiple Meningioma
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MNGMA
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Meningioma, Benign, No Icd-O Subtype
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Intracranial Meningioma
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Meningothelial Cell Neoplasm
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Supratentorial Meningioma
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Primary Neoplasm Of Spinal Meninges
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Benign Intracranial Meningioma
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Benign Meningioma
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Meningeal Tumours
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Meningeal Sarcoma Of Unspecified Site
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Meningothelial Sarcoma Of Unspecified Site
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Congenital Nervous System Abnormality |
Congenital Neurologic Anomaly
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Congenital Nervous System Disorder
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Strabismus |
Strabismus, Susceptibility To
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Strabismus, Susceptibility To, 1
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Strabismus 1
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Skin Disease |
Skin Diseases
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Genodermatosis
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Abnormality Of The Skin
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Skin Diseases, Genetic
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Skin And Subcutaneous Tissue Disease
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Dermatologic Disorders
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Interstitial Lung Disease 2 |
Idiopathic Pulmonary Fibrosis
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Ipf
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Fibrocystic Pulmonary Dysplasia
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Pulmonary Fibrosis, Idiopathic
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Pulmonary Fibrosis, Idiopathic, Susceptibility To
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Cryptogenic Fibrosing Alveolitis
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ILD2
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Idiopathic Pulmonary Fibrosis, Familial
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Fibrosing Alveolitis, Cryptogenic
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Uip
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Fibrosing Alveolitis
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Interstitial Pneumonitis, Usual
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Familial Idiopathic Pulmonary Fibrosis
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Idiopathic Fibrosing Alveolitis, Chronic Form
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Usual Interstitial Pneumonia
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Fibrosing Alveolitis Cryptogenic
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Hamman-Rich Disease
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Idiopathic Pulmonary Fibrosis Familial
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Interstitial Pneumonitis Usual
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Fibrosis Idiopathic Pulmonary
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Fibrosis, Pulmonary, Idiopathic
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Hamman-Rich Syndrome
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Chronic Idiopathic Pulmonary Fibrosis
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Acute Interstitial Pneumonia
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Interstitial Pulmonary Fibrosis
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Ipf - [Idiopathic Pulmonary Fibrosis]
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Idiopathic Lung Fibrosis
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Fibrosing Lung Disease
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Pulmonary Fibrosis Nos
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Fibrosing Pneumonitis
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Wilms Tumor 1 |
Nephroblastoma
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Wilms Tumor
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WT1
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Wilms' Tumor
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Bilateral Wilms Tumor
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Wilms Tumor, Type 1
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Wilms Tumor, Somatic
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Adult Nephroblastoma
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Wt1 Disorder
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Renal Embryonic Tumor
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Adult Kidney Wilms Tumor
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Childhood Kidney Wilms Tumor
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Nonanaplastic Kidney Wilms Tumor
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Dilated Cardiomyopathy |
Familial Dilated Cardiomyopathy
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Primary Dilated Cardiomyopathy
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Idiopathic Dilated Cardiomyopathy
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Congestive Cardiomyopathy
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Idiopathic Dilation Cardiomyopathy
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Primary Familial Dilated Cardiomyopathy
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Cardiomyopathy, Dilated
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DCM
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Cardiomyopathy, Familial Dilated
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Dilated Cardiomyopathy, Familial
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Hypokinetic Dilated Cardiomyopathy, Familial
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Familial Idiopathic Cardiomyopathy
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Fdc
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Cardiomyopathy, Familial Idiopathic
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Idiopathic Cardiomegaly
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Dilated Congestive Cardiomyopathy
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Chronic Dilated Cardiomyopathy
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Ccm - [Congestive Cardiomyopathy]
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Cocm - [Congestive Cardiomyopathy]
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Dcm - [Dilated Cardiomyopathy]
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Dilated-Hypokinetic Cardiomyopathy
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Congestive Idiopathic Cardiomyopathy
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Primary Idiopathic Dilated Cardiomyopathy
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Hypertrophic Cardiomyopathy |
Hypertrophic Obstructive Cardiomyopathy
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Cardiomyopathy, Hypertrophic
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Cardiomyopathy Hypertrophic Obstructive
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Cardiomyopathy, Hypertrophic, Familial
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Idiopathic Myocardial Hypertrophy
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Idiopathic Hypertrophic Cardiomyopathy
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Obstructive Idiopathic Hypertrophic Cardiomyopathy
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Obstructive Cardiomyopathy
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Idiopathic Hypertrophic Subaortic Stenosis
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Muscular Subaortic Stenosis
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Hypertrophic Obstructive Subaortic Stenosis
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Alzheimer Disease, Familial, 1 |
Alzheimer Disease
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Alzheimer'S Disease
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Presenile And Senile Dementia
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AD1
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Alzheimer Disease, Susceptibility To
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Alzheimer Disease, Late-Onset, Susceptibility To
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Alzheimer Disease 1, Familial
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AD
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Familial Alzheimer Disease
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Alzheimer Disease, Late-Onset
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Alzheimers Dementia
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Alzheimer Dementia
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Alzheimer Sclerosis
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Alzheimer Syndrome
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Alzheimer-Type Dementia
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Dat
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Primary Senile Degenerative Dementia
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Sdat
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Alzheimer Disease 1
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Autosomal Dominant Alzheimer Disease
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Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
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Late Onset Alzheimer Disease
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Alzheimers Disease
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Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
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Late-Onset Alzheimers Disease
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Alzheimer'S Disease Pathway Kegg
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Dementia Due To Alzheimer'S Disease
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Alzheimer Disease Type 1
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Alzheimers
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Retinitis Pigmentosa |
RP
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Rod-Cone Dystrophy
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Autosomal Recessive Retinitis Pigmentosa
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Non-Syndromic Retinitis Pigmentosa
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Pericentral Pigmentary Retinopathy
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Pigmentary Retinopathy
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Tapetoretinal Degeneration
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Rcd
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Retinitis Pigmentosa Autosomal Recessive
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ARRP
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Retinitis Pigmentosa, Autosomal Recessive
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Retinitis Pigmentosa 1
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Fundus Dystrophy |
Retinal Dystrophy
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Retinal Dystrophies
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Dystrophy, Retinal
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