疾病名称 |
别名 |
|
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
|
|
|
Overnutrition |
|
|
Eating Disorder |
Eating Disorders
|
Feeding And Eating Disorders
|
|
|
Bulimia Nervosa |
Bulimia
|
Bulimia Nervosa, Susceptibility To
|
Binge Eating Disorder
|
BULN
|
Bn
|
Hyperorexia Nervosa
|
Bulimia Nervosa 2
|
BULN2
|
Susceptibility To Bulimia Nervosa
|
Bulimia Nervosa, Susceptibility To, Type 2
|
Bn - [Bulimia Nervosa]
|
Bulimia Nos
|
Bulimic
|
Bingeing
|
Binge Overeating
|
Bouts Of Overeating
|
Episodes Of Overeating
|
|
|
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
|
|
|
Severe Pre-Eclampsia |
Severe Preeclampsia
|
Antepartum Severe Pre-Eclampsia
|
Postpartum Severe Pre-Eclampsia
|
Severe Pre-Eclampsia, With Delivery
|
Severe Toxemia
|
Severe Pre-Eclampsia, Antepartum Condition Or Complication
|
Severe Pre-Eclampsia, Postpartum Condition Or Complication
|
Severe Puerperal Pre-Eclampsia
|
Severe Pre-Eclamptic Toxaemia
|
Severe Pet - [Pre-Eclamptic Toxaemia]
|
|
|
Glucose Intolerance |
Glucose: Intolerance
|
Glucose: Malabsorption
|
Malabsorption Of Glucose
|
Impaired Glucose Tolerance
|
|
|
Anorexia Nervosa |
Anorexia Nervosa, Susceptibility To
|
ANON
|
Anorexia Nervosa, Susceptibility To, 1
|
An
|
Anorexia Nervosa 1
|
An - [Anorexia Nervosa]
|
|
|
Sleep Apnea |
|
|
Hyperinsulinism |
|
|
Acquired Generalized Lipodystrophy |
Lawrence Syndrome
|
Acquired Lipoatrophic Diabetes
|
Lawrence-Seip Syndrome
|
Familial Generalized Lipodystrophy
|
|
|
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
|
|
|
Nutritional Deficiency Disease |
Malnutrition
|
Nutritional Disorder
|
Nutritional Deficiency
|
Nutrition
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
Nutrition Disorders
|
|
|
Hypogonadism |
|
|
Protein-Energy Malnutrition |
PEM
|
Protein Energy Malnutrition
|
|
|
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
|
|
|
Acanthosis Nigricans |
|
|
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
|
|
|
Familial Partial Lipodystrophy |
Lipodystrophy, Familial Partial
|
Fpld
|
Kobberling-Dunnigan Syndrome
|
Dunnigan Syndrome
|
Koberling-Dunnigan Syndrome
|
Dunnigan-Kobberling Syndrome
|
Fpl
|
Familial Partial Lipodystrophy, Type 2
|
|
|
Abdominal Obesity-Metabolic Syndrome 1 |
Metabolic Syndrome X
|
Metabolic Syndrome
|
AOMS1
|
Dysmetabolic Syndrome X
|
Metabolic Disease
|
Abdominal Obesity Metabolic Syndrome
|
|
|
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
|
|
|
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]
|
|
|
Hyperglycemia |
|
|
Liver Disease |
Liver Failure
|
Liver Diseases
|
Abnormality Of The Liver
|
Liver Dysfunction
|
Disorder Of Liver
|
Hepatic Disorder
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
Liver Function Failure
|
Hepatic Failure Nos
|
Liver Failure Nos
|
End Stage Liver Disease
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
Liver Necrosis With Hepatic Failure
|
|
|
Sick Building Syndrome |
|
|
Lipodystrophy, Familial Partial, Type 2 |
FPLD2
|
Lipoatrophic Diabetes
|
Familial Partial Lipodystrophy Type 2
|
Familial Partial Lipodystrophy, Dunnigan Type
|
Fpl2
|
Lipoatrophic Diabetes Mellitus
|
Lipodystrophy, Familial Partial, Dunnigan Type
|
Lipodystrophy, Familial, Of Limbs And Lower Trunk
|
Lipodystrophy, Reverse Partial
|
Familial Partial Lipodystrophy Dunnigan Type
|
Dunnigan Syndrome
|
Familial Lipodystrophy Of Limbs And Lower Trunk
|
Reverse Partial Lipodystrophy
|
Lipodystrophy, Familial Partial, 2
|
Generalized Lipoatrophy Associated With Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy And Leukomelanodermic Papules
|
Lipodystrophy Familial Of Limbs And Lower Trunk
|
Lipodystrophy Reverse Partial
|
Diabetes Mellitus, Lipoatrophic
|
Familial Partial Lipodystrophy, Type 2
|
Familial Generalized Lipodystrophy
|
|
|
Uremia |
|
|
Placental Insufficiency |
Uteroplacental Vascular Insufficiency
|
|
|
Myoma |
Muscle Benign Neoplasm
|
Myomatous Neoplasm
|
Neoplasms, Muscle Tissue
|
Benign Neoplasm Of The Muscle
|
Muscle Neoplasm
|
Muscle Tissue Neoplasm
|
Myomatous Tumor
|
Neoplasm Of Muscle
|
Muscle Neoplasms
|
Myomas
|
|
|
Congenital Generalized Lipodystrophy |
Berardinelli-Seip Congenital Lipodystrophy
|
Berardinelli-Seip Syndrome
|
Brunzell Syndrome
|
Bscl
|
Generalized Lipodystrophy
|
Lipodystrophy, Congenital Generalized
|
Seip Syndrome
|
Total Lipodystrophy
|
Cgl
|
Lipoatrophic Diabetes
|
Lipodystrophy, Generalized, Congenital
|
Familial Generalized Lipodystrophy
|
Congenital Generalized Lipodystrophy Type 2
|
Lipoatrophic Diabetes Mellitus
|
Familial Partial Lipodystrophy, Type 2
|
|
|
Spinal Cord Injury |
|
|
Hyperthyroidism |
|
|
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
|
|
|
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
|
|
|
Diabetes Mellitus |
|
|
Amenorrhea |
Absence Of Menstruation
|
Amenia
|
|
|
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
|
|
|
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
|
|
|
Lipedema |
|
|
Acquired Metabolic Disease |
|
|
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
|
|
|
Hypothyroidism |
Thyroid Diseases
|
Thyroid Disease
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
Narcolepsy |
Paroxysmal Sleep
|
Gelineau Syndrome
|
Narcoleptic Syndrome
|
Narcolepsy-Cataplexy Syndrome
|
Cataplexy And Narcolepsy
|
Narcolepsy, Without Cataplexy
|
Gelineau'S Syndrome
|
Narcolepsy With Or Without Cataplexy
|
Narcolepsy Nos
|
|
|
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
|
|
|
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
|
|
|
Cardiovascular System Disease |
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
Cardiovascular Diseases
|
|
|
Acromegaly |
Gigantism
|
Growth Hormone Excess
|
Pituitary Giant
|
Somatotroph Adenoma
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
|
Complete Generalized Lipodystrophy |
|
|
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
|
|
|
Anovulation |
|
|
Complement Component 9 Deficiency |
C9 Deficiency
|
C9D
|
C9 Deficiency With Dermatomyositis
|
|
|
Liver Cirrhosis |
Cirrhosis
|
Cirrhosis Of Liver
|
CIRRH
|
Cryptogenic Cirrhosis
|
Cirrhosis, Cryptogenic
|
Cirrhosis Nos
|
|
|
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
|
|
|
Sleep Disorder |
Sleep Disorders
|
Non-Organic Sleep Disorder
|
|
|
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
|
|
|
Cholelithiasis |
|
|
Pseudohypoparathyroidism |
Familial Pseudohypoparathyroidism
|
Parathyroid Hormone Resistant Hypoparathyroidism
|
Php - [Pseudohypoparathyroidism]
|
Constitutional Chronic Hypocalcaemia
|
|
|
Short Bowel Syndrome |
Short Gut Syndrome
|
Acquired Short Bowel Syndrome
|
Secondary Short Bowel Syndrome
|
Short Bowel Nos
|
|
|
Major Depressive Disorder |
Seasonal Affective Disorder
|
Unipolar Depression
|
Depression
|
MDD
|
Depressive Disorder
|
Unipolar Depression, Susceptibility To
|
Major Depressive Disorder 1
|
Major Depressive Disorder, Response To Citalopram Therapy In
|
Major Depressive Disorder 2
|
Winter Depression
|
Single Major Depressive Episode
|
Sad
|
Clinical Depression
|
Major Depression
|
Depressive Syndrome
|
Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment
|
Seasonal Affective Disorder, Susceptibility To
|
Recurrent Major Depression
|
Affective Disorder, Seasonal
|
Depression In A Seasonal Pattern
|
Depression
|
Seasonal
|
Major Depressive Disorder With A Seasonal Pattern
|
Seasonal Depression
|
Seasonal Mood Disorder
|
Mental Depression
|
Recurrent Major Depressive Episodes
|
|
|
Hyperuricemia |
Blood Urate Raized
|
Uricacidemia
|
|
|
Muscle Hypertrophy |
MSLHP
|
Hypertrophy
|
Hypertrophy, Muscle
|
|
|
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
|
|
|
Obesity-Hypoventilation Syndrome |
Obesity Hypoventilation Syndrome
|
Pickwickian Syndrome
|
Cardiopulmonary Obesity Syndrome
|
Extreme Obesity With Alveolar Hypoventilation With Body-Mass-Index Unspecified
|
Alveolar Hypoventilation Syndrome
|
Alveolus Hypoventilation Syndrome
|
Ohs - [Obesity Hypoventilation Syndrome]
|
|
|
Pericarditis |
|
|
Gynecomastia |
|
|
Hypoplastic Left Heart Syndrome |
Hlhs
|
Heart, Hypoplastic Left, Syndrome
|
Hypoplasia Of The Left Heart
|
Left Heart Hypoplasia Syndrome
|
Hlhs - [Hypoplastic Left Heart Syndrome]
|
Hypoplasia Of Aortic Valve, In Hypoplastic Left Heart Syndrome
|
Atresia Of Mitral Valve, In Hypoplastic Left Heart Syndrome
|
Atresia Or Marked Hypoplasia Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle
|
Atresia Or Marked Hypoplasia, Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle With Mitral Valve Atresia
|
Aortic Valve Atresia, In Hypoplastic Left Heart Syndrome
|
Ascending Aorta Hypoplasia, In Hypoplastic Left Heart Syndrome
|
|
|
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
|
|
|
Familial Hyperlipidemia |
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
Hyperlipoproteinemias
|
Hyperlipidemia
|
Hyperlipemia
|
Hyperlipidemias
|
|
|
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
|
|
|
Varicocele |
Scrotal Varices
|
Varicoceles
|
Varicocele Of Scrotum
|
Scrotal Varicocele
|
|
|
Fibromyalgia |
Diffuse Myofascial Pain Syndrome
|
Fibromyalgia Syndrome
|
Fibromyalgia-Fibromyositis Syndrome
|
Fibromyositis
|
Fibrositis
|
Fms
|
Myofascial Pain Syndrome
|
Myofascial Pain Syndromes
|
|
|
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
|
|
|
Atherosclerosis Susceptibility |
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
Alp
|
Arteriosclerosis
|
|
|
Ovarian Disease |
Ovarian Dysfunction
|
Ovarian Diseases
|
Ovarian Disorders
|
Disorder Of Endocrine Ovary
|
|
|
Relapsing-Remitting Multiple Sclerosis |
Relapsing-Remitting Ms
|
Relapsing Remitting Multiple Sclerosis
|
Multiple Sclerosis, Relapsing-Remitting
|
Rrms
|
Multiple Sclerosis Relapsing-Remitting
|
|
|
Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
Abdominal Obesity-Metabolic Syndrome
|
Abdominal Obesity Metabolic Syndrome
|
Metabolic Syndrome X
|
Aoms2
|
Aoms1
|
|
|
Hellp Syndrome |
Hemolysis, Elevated Liver Enzymes, Lowered Platelets
|
Hemolysis, Elevated Liver Enzymes, Low Platelets In Pregnancy
|
Hemolysis-Elevated Liver Enzymes-Low Platelets Syndrome
|
Hellp - [Syndrome Of Haemolysis, Elevated Liver Enzymes And Low Platelet]
|
Haemolysis-Elevated Liver Enzymes-Low Platelet Count Syndrome
|
|
|
Lipodystrophy, Congenital Generalized, Type 2 |
Congenital Generalized Lipodystrophy Type 2
|
CGL2
|
Berardinelli-Seip Congenital Lipodystrophy Type 2
|
Berardinelli-Seip Syndrome
|
Brunzell Syndrome Bscl2-Related
|
Total Lipodystrophy And Acromegaloid Gigantism
|
Berardinelli-Seip Congenital Lipodystrophy, Type 2
|
Seip Syndrome
|
Berardinelli Syndrome
|
Lipodystrophy, Total, And Acromegaloid Gigantism
|
Lipoatrophic Diabetes, Congenital
|
Lipodystrophy, Berardinelli-Seip Congenital, Type 2
|
Brunzell Syndrome, Bscl2-Related
|
Congenital Lipoatrophic Diabetes
|
Congenital Generalized Lipodystrophy 2
|
Lipoatrophic Diabetes
|
Lipodystrophy Berardinelli Type
|
Familial Generalized Lipodystrophy
|
Lipoatrophic Diabetes Mellitus
|
Familial Partial Lipodystrophy, Type 2
|
|
|
Acne |
Acne Vulgaris
|
Acne Varioliformis
|
Frontalis Acne
|
|
|
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
|
|
|
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
|
|
|
Infertility |
|
|
Kidney Disease |
Renal Failure
|
Kidney Failure
|
Kidney Diseases
|
Nephropathy
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
Renal Anomaly
|
Kidney Dysfunction
|
Renal Disease
|
Nephropathies
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
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
|
|
|
Blount'S Disease |
Blount Disease
|
Tibia Vara
|
Osteochondrosis Deformans Tibiae
|
Osteochondrosis Deformans Tibiae, Familial Infantile Type
|
Familial Infantile Type Osteochondrosis Deformans Tibiae
|
Blount-Barber Syndrome
|
Erlacher-Blount Syndrome
|
Infantile Tibia Vara
|
Tibia Vara Blount
|
Blount Disease, Infantile
|
|
|
Takayasu Arteritis |
Aortic Arch Syndrome
|
Pulseless Disease
|
Takayasu'S Arteritis
|
Idiopathic Aortitis
|
Young Female Arteritis
|
Aortic Arch Arteritis
|
Aortic Arches Defect
|
Aortic Arch Defects
|
Takayasu Disease
|
Aortic Arch Syndromes
|
Takayasu'S Disease
|
Ta
|
Obliterative Aortitis
|
Aortic Arch Giant-Cell Arteritis
|
Subclavian-Carotid Obstruction Syndrome
|
Idiopathic Medial Aortopathy And Arteriopathy
|
Takayasu Syndrome
|
Obliterative Brachiocephalic Arteritis Syndrome
|
Raeder-Harbitz Syndrome
|
Chronic Subclavian-Carotid Obstruction Syndrome
|
Giant-Cell Aortitis
|
Takayasu Aortitis
|
Nonspecific Aortoarteritis
|
Sclerosing Aortitis And Arteritis
|
Martorell 2 Syndrome
|
Young Female Aortic Arch Arteritis Syndrome
|
|
|
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
|
|
|
Homocystinuria |
Cystathionine Beta Synthase Deficiency
|
Homocysteinemia
|
Cbs Deficiency
|
Cystathionine Synthase Deficiency
|
Cystathionine Beta-Synthase Deficiency Disease
|
|
|
Bardet-Biedl Syndrome |
Bbs
|
Biedl-Bardet Syndrome
|
|
|
Hypoglycemia |
Hypoglycaemia
|
Low Blood Sugar
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
Hypoglycaemic Syndrome
|
|
|
Non-Alcoholic Steatohepatitis |
Nonalcoholic Steatohepatitis
|
Nash
|
Nash - [Non-Alcoholic Steatohepatitis]
|
Non-Alcoholic Steatohepatosis
|
|
|
Lipid Storage Disease |
Lipoidosis
|
Inborn Lipid Storage Disorder
|
Lipoid Storage Diseas
|
Lipid Storage Diseases
|
Lipidoses
|
|
|
Skin Tag |
Fibroepithelial Polyp
|
Fibroepithelial Polyp Of Skin
|
Soft Fibroma
|
Skin Tags
|
Cutaneous Tag
|
Gardner Fibroma
|
Acrochordon
|
Fibroma Molle
|
|
|
Obsessive-Compulsive Disorder |
OCD
|
Obsessive-Compulsive Disorder, Susceptibility To
|
Anancastic Neurosis
|
Obsessive Compulsive Disorder
|
Anankastic Neurosis
|
Obsessive-Compulsive Neurosis
|
Obsessive Compulsive Behavior
|
|
|
Diencephalic Astrocytoma |
Astrocytoma Of Diencephalon
|
|
|
Hypogonadism, Male |
Male Hypogonadism
|
Hypogonadism Male
|
Testicular Hypogonadism
|
|
|
Muscular Atrophy |
Muscle Wasting
|
Amyotrophia
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
Diarrhea |
Diarrhoea
|
Diarrhea Of Presumed Infectious Origin
|
|
|
Scoliosis |
|
|
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
|
|
|
Intracranial Hypertension, Idiopathic |
Pseudotumor Cerebri
|
Idiopathic Intracranial Hypertension
|
Benign Intracranial Hypertension
|
Iih
|
Benign Intracran. Hypt.
|
|
|
Vascular Disease |
Vascular Diseases
|
Aneurysm
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
Inherited Metabolic Disorder |
Inborn Errors Of Metabolism
|
Inborn Metabolic Disorder
|
Inborn Metabolism Disorder
|
Metabolic Hereditary Disorder
|
Inborn Error Of Metabolism
|
Metabolism, Inborn Errors
|
|
|
Alcohol Dependence |
Alcoholism
|
Alcohol Dependence, Susceptibility To
|
Alcohol Dependence, Protection Against
|
Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against
|
Alcoholism, Susceptibility To
|
Alcoholic Intoxication, Chronic
|
Pharyngeal Neoplasms
|
Chronic Alcoholism
|
Dipsomania
|
Alcohol Addiction
|
Ethanol Dependence
|
Chronic Ethanolism
|
Chronic Alcoholic Disease Nos
|
Alcoholic Disease Nos
|
Alcoholic
|
|
|
Asthma |
Chronic Obstructive Asthma
|
Asthma, Diminished Response To Antileukotriene Treatment In
|
Bronchial Hyperreactivity
|
Asthma, Susceptibility To
|
Asthma, Bronchial
|
Asthma, Protection Against
|
Asthma, Nocturnal, Susceptibility To
|
Nocturnal Asthma
|
Asthma-Related Traits
|
Asthma-Related Traits, Susceptibility To
|
Asthma, Nocturnal
|
Chronic Obstructive Asthma With Acute Exacerbation
|
Chronic Obstructive Asthma With Status Asthmaticus
|
Exercise Induced Asthma
|
Exercise-Induced Asthma
|
Bronchial Asthma
|
Asthma, Exercise-Induced
|
Idiosyncratic Asthma
|
Unspecified Asthma With Acute Exacerbation
|
Asthma, Unspecified, With Stated Status Asthmaticus
|
Status Asthmaticus Nos
|
Acute Severe Asthma
|
Acute Severe Bronchial Asthma
|
Status Asthma
|
Status Post Asthmaticus
|
|
|
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
|
|
|
Lipodystrophy, Familial Partial, Type 3 |
FPLD3
|
Pparg-Related Familial Partial Lipodystrophy
|
Familial Partial Lipodystrophy Type 3
|
Familial Partial Lipodystrophy Associated With Pparg Mutations
|
Pparg-Related Fpld
|
Lipodystrophy, Familial Partial, Associated With Pparg Mutations
|
Insulin Resistance, Severe, Digenic
|
Lipodystrophy, Familial Partial, 3
|
Familial Partial Lipodystrophy, Type 3
|
|
|
Atypical Depressive Disorder |
|
|
Marasmus |
Nutritional Marasmus
|
Nutritional Atrophy
|
|
|
Mild Pre-Eclampsia |
|
|
Central Precocious Puberty |
Cpp
|
Gonadotropin-Dependant Precocious Puberty
|
Gonadotropin-Dependent Precocious Puberty
|
Precocious Puberty, Central
|
|
|
Kallmann Syndrome |
Hypogonadism With Anosmia
|
Kallman'S Syndrome
|
Anosmic Hypogonadism
|
Anosmic Idiopathic Hypogonadotropic Hypogonadism
|
Hypogonadotropic Hypogonadism And Anosmia
|
Hypogonadotropic Hypogonadism-Anosmia Syndrome
|
Olfacto-Genital Pathological Sequence
|
Familial Hypogonadism With Anosmia
|
Kallman Syndrome
|
Dysplasia Olfactogenitalis Of De Morsier
|
Kallmann'S Syndrome
|
Congenital Hypogonadotropic Hypogonadism With Anosmia
|
|
|
Pigmentation Disease |
Pigmentation Disorders
|
Skin Pigmentation Disorder
|
|
|
Anxiety |
Anxiety Disorder
|
Anxiety Disorders
|
Anxiety State
|
Anxieties
|
Anxiety Neurosis
|
|
|
Donohue Syndrome |
Leprechaunism
|
Leprechaunism Syndrome
|
Donohue'S Syndrome
|
LEPRCH
|
|
|
Adermatoglyphia |
ADERM
|
Immigration Delay Disease
|
Absence Of Fingerprints
|
Adg
|
Congenital Absence Of Fingerprints
|
Isolated Congenital Adermatoglyphia
|
Fingerprints, Absence Of
|
Skin Abnormalities
|
|
|
Central Sleep Apnea |
Central Sleep Apnea Syndrome
|
Sleep Apnea, Central
|
Primary Central Sleep Apnea
|
Central Sleep Apnea, Primary
|
Central Sleep Apnoea Syndrome
|
Csa - [Central Sleep Apnoea]
|
Csas - [Central Sleep Apnoea Syndrome]
|
Central Sleep Apnoea Due To Substances Including Medications
|
|
|
Specific Developmental Disorder |
|
|
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
|
|
|
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
|
|
|
Kwashiorkor |
Kwashiokor
|
Nutritional Edema With Dyspigmentation Of Skin And Hair
|
Nutritional Oedema With Dyspigmentation Of Skin And/Or Hair
|
|
|
Cerebral Palsy |
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
Palsy Cerebral
|
Palsy, Cerebral
|
Cerebral Palsy, Mixed
|
|
|
Hernia, Hiatus |
Hiatal Hernia
|
Hiatus Hernia
|
Diaphragmatic - Hiatus -Hernia
|
Hernia, Hiatal
|
|
|
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
|
|
|
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
|
|
|
Lysosomal Storage Disease |
Lysosomal Storage Diseases
|
Disorder Of Lysosomal Enzyme
|
Inborn Lysosomal Enzyme Disorder
|
Lysosomal Storage Metabolism Disorder
|
Lysosomal Storage Disorder
|
|
|
Frontotemporal Dementia |
Pallidopontonigral Degeneration
|
Frontotemporal Lobar Degeneration
|
Semantic Dementia
|
FTD
|
Frontotemporal Lobe Dementia
|
Multiple System Tauopathy With Presenile Dementia
|
Dementia, Frontotemporal
|
Frontotemporal Dementia With Parkinsonism
|
Mstd
|
Frontotemporal Lobar Degeneration With Tau Inclusions
|
Ftld With Tau Inclusions
|
Dementia, Frontotemporal, With Parkinsonism
|
Fldem
|
Ftdp17
|
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
|
Ddpac
|
Wilhelmsen-Lynch Disease
|
Wld
|
Ppnd
|
Dementia, Frontotemporal, With Or Without Parkinsonism
|
Semantic Primary Progressive Aphasia
|
Semantic Variant Ppa
|
Wilhemsen-Lynch Disease
|
Frontotemporal Dementia-Amyotrophic Lateral Sclerosis
|
Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17
|
Ftd-Als
|
Ftld
|
Pick Complex
|
Pick Disease Of The Brain
|
Frontotemporal Dementia With Parkinsonism-17
|
Grn-Related Frontotemporal Dementia
|
Frontotemporal Dementia With Motor Neuron Disease
|
Dementia In Fronto-Temporal Lobar Degeneration
|
Ftd - [Frontotemporal Dementia]
|
Temple Dementia
|
Frontal Lobe Dementia
|
|
|
Fetal Macrosomia |
|
|
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
|
|
|
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
|
|
|
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
|
|
|
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
|
|
|
Thyroid Gland Disease |
Abnormality Of The Thyroid Gland
|
Thyroid Diseases
|
|
|
Inflammatory Bowel Disease |
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
Palmoplantar Keratoderma, Punctate Type Iii |
Acrokeratoelastoidosis Of Costa
|
Ake
|
Punctate Palmoplantar Keratoderma Type Iii
|
PPKP3
|
Keratoderma, Palmoplantar, Punctate Type 3
|
Punctate Palmoplantar Hyperkeratosis Type 3
|
Punctate Palmoplantar Keratoderma Type 3
|
Rare Form Of Hirschsprung'S Disease
|
Acrokeratoelastoidosis
|
Collagenous Plaques Of Hands And Feet
|
Aganglionosis, Total Intestinal
|
Collagenous Plaques Of Hand And Feet
|
Palmoplantar Keratoderma, Punctate Type 3
|
Aganglionosis, Total Colonic
|
Ntia
|
Near-Total Intestinal Aganglionosis
|
Tia
|
|
|
Autoimmune Disease Of Endocrine System |
|
|
Disease Of Mental Health |
Mental Health
|
Mental Disorders
|
|
|
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
|
|
|
Acute Promyelocytic Leukemia |
Leukemia, Acute Promyelocytic
|
Acute Myeloblastic Leukemia Type 3
|
Aml M3
|
APL
|
Leukemia, Acute Promyelocytic, Somatic
|
Aml With T(15
|
17)(Q22
|
Q12)
|
(Pml/Raralpha) And Variants
|
Apml
|
Acute Myeloblastic Leukemia 3
|
Acute Myeloid Leukemia With T(15
|
17)(Q22
|
Q12)
|
(Pml/Raralpha) And Variants
|
Acute Myeloblastic Leukaemia Type 3
|
Acute Myeloid Leukaemia M3
|
Acute Myeloid Leukemia M3
|
Acute Promyelocytic Leukaemia
|
M3 Anll
|
Myeloid Leukemia, Acute, M3
|
Leukemia Promyelocytic Acute
|
Leukemia, Promyelocytic, Acute
|
Leukemia, Acute, Promyelocytic
|
|
|
Schizophrenia |
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
Schizophrenia-1
|
Dementia Praecox
|
Schizophrenia 1
|
|
|
Deficiency Anemia |
Anemia
|
Deficiency Anemias
|
Anaemia
|
|
|
Autism |
Autistic Disorder
|
Autism Susceptibility 1
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
Kanner'S Syndrome
|
Autistic
|
|
|
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
|
|
|
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
|
|
|
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
|
|
|
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
|
|
|
Maturity-Onset Diabetes Of The Young |
MODY
|
Maturity Onset Diabetes Mellitus In Young
|
Mason-Type Diabetes
|
Mason Type Diabetes
|
Maturity Onset Diabetes Of The Young
|
Mody Syndrome
|
Diabetes Of The Young, Maturity-Onset
|
|
|
Migraine With Or Without Aura 1 |
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
Migraine Disorder
|
Migraine Variant
|
Migraines
|
Migraine Disorders
|
Mgr1
|
Mgau
|
Ma
|
Migraine With Or Without Aura
|
Classic Migraine
|
Common Migraine
|
Disorder, Migraine
|
Headache Migraine
|
Headache Migrainous
|
Migraine Headache
|
Migraine Syndrome
|
Headache Including Migraine
|
Migraine, Susceptibility To
|
|
|
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
|
|
|
Connective Tissue Disease |
Connective Tissue Diseases
|
Connective Tissue Disorder
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
Connective Tissue Disorders
|
|
|
Attention Deficit-Hyperactivity Disorder |
Attention Deficit Hyperactivity Disorder
|
ADHD
|
Attention Deficit Disorder
|
Attention Deficit-Hyperactivity Disorder, Susceptibility To
|
Attention Deficit Disorder With Hyperactivity
|
Hyperkinetic Disorder
|
Hyperactivity Of Childhood
|
Attention-Deficit/Hyperactivity Disorder
|
Add
|
Addh
|
Attention Deficit
|
Attention Deficit Disorder Of Childhood With Hyperactivity
|
Attention Deficit Disorder With Hyperactivity Syndrome
|
Hyperkinetic Syndrome
|
Attention-Deficit Hyperactivity Disorder
|
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
|
Disturbance Of Activity And Attention
|
Disorder Of Activity And Attention
|
Adhd - [Attention Deficit Hyperactivity Disorder]
|
Hyperkinetic Disorders
|
Disorder Of Activity And Attention With Hyperkinesia
|
Attention Deficit Syndrome With Hyperactivity
|
|
|
Peripheral Nervous System Disease |
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
Nervous System Disease |
Abnormality Of The Nervous System
|
Nervous System Diseases
|
Nervous System Disorder
|
|
|