| 疾病名称 |
别名 |
|
| 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
|
|
|
| Growth Hormone Insensitivity, Partial |
|
Short Stature Due To Partial Ghr Deficiency
|
GHIP
|
|
Increased Responsiveness To Growth Hormone
|
Short Stature Due To Partial Growth Hormone Receptor Deficiency
|
|
Isolated Partial Growth Hormone Deficiency
|
Partial Ighd
|
|
Short Stature, Idiopathic, Autosomal
|
|
|
| Hypercholesterolemia, Familial, 1 |
|
Hypercholesterolemia
|
FHCL1
|
|
Fhc
|
Fh
|
|
Hyperlipoproteinemia, Type Ii
|
Hyperlipoproteinemia, Type Iia
|
|
Hyper-Low-Density-Lipoproteinemia
|
Hypercholesterolemic Xanthomatosis, Familial
|
|
Ldl Receptor Disorder
|
Hypercholesterolemia, Susceptibility To
|
|
Hypercholesterolemia, Familial, Modifier Of
|
Hypercholesterolemia, Familial, Due To Ldlr Defect, Modifier Of
|
|
Ldl Cholesterol Level Qtl2
|
Hyperlipoproteinemia Type Ii
|
|
Hypercholesterolemia, Familial, Type 1
|
High Cholesterol
|
|
Increased Cholesterol
|
Low-Density-Lipoid-Type Hyperlipoproteinemia
|
|
Pure Hypercholesterolaemia
|
Ldl - [Low Density Lipoprotein} Hyperlipoproteinemia
|
|
Group A Hyperlipidaemia
|
Pure Hypercholesterinaemia
|
|
Cholesterolaemia
|
Essential Cholesterolaemia
|
|
Essential Hypercholesterolaemia
|
Group A Hyperlipemia
|
|
Increased Low Density Lipoprotein
|
Low-Density-Lipoprotein-Type
|
|
Low-Density-Lipoprotein-Type Hyperlipoproteinemia
|
|
|
| Growth Hormone Deficiency, Isolated Partial |
|
Short Stature Due To Growth Hormone Secretagogue Receptor Deficiency
|
GHDP
|
|
Short Stature Due To Ghsr Deficiency
|
Ghrelin Receptor Deficiency
|
|
Hormone, Growth, Deficiency, Isolated Partial
|
Short Stature, Idiopathic, Autosomal
|
|
|
| Specific Learning Disability |
|
Specific Learning Difficulty
|
Specific Learning Disorder
|
|
|
| Acromegaly |
|
Gigantism
|
Growth Hormone Excess
|
|
Pituitary Giant
|
Somatotroph Adenoma
|
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
|
| 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
|
|
|
| Familial Hypercholesterolemia |
|
Hyperlipoproteinemia Type Iia
|
Familial Hyperbetalipoproteinaemia
|
|
Familial Hypercholesteremia
|
Fredrickson Type Iia Hyperlipoproteinemia
|
|
Fredrickson Type Iia Lipidaemia
|
Hyperbetalipoproteinemia
|
|
Type Ii Hyperlipidemia
|
Familial Hypercholesterolæmia
|
|
Familial Hypercholesterolaemia
|
Fh
|
|
Hypercholesterolemia Familial
|
Hyperlipoproteinemia Type Ii
|
|
Hypercholesterolemia, Familial
|
|
|
| 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
|
|
|
| Uremia |
|
|
| Anorexia Nervosa |
|
Anorexia Nervosa, Susceptibility To
|
ANON
|
|
Anorexia Nervosa, Susceptibility To, 1
|
An
|
|
Anorexia Nervosa 1
|
An - [Anorexia Nervosa]
|
|
|
| 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
|
|
|
| Actinic Keratosis |
|
Solar Keratosis
|
Actinic Keratosis
|
|
Senile Hyperkeratosis
|
Sk - Solar Keratosis
|
|
Keratosis, Actinic
|
Seborrheic Keratosis
|
|
Ak - [Actinic Keratosis]
|
Sk - [Solar Keratosis]
|
|
|
| Pituitary Adenoma |
|
Adenoma Of The Pituitary Gland
|
Pituitary Adenomas
|
|
Adenoma, Pituitary
|
Pituitary Gland Adenoma
|
|
Pituitary Neoplasms
|
|
|
| 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
|
|
|
| Schizophrenia 11 |
|
Sczd11
|
Schizophrenia Susceptibility Locus, Chromosome 10q-Related
|
|
|
| Hypoglycemia |
|
Hypoglycaemia
|
Low Blood Sugar
|
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
|
Hypoglycaemic Syndrome
|
|
|
| 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
|
|
|
| Hyperpituitarism |
|
|
| Familial Hyperlipidemia |
|
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
|
Hyperlipoproteinemias
|
Hyperlipidemia
|
|
Hyperlipemia
|
Hyperlipidemias
|
|
|
| Hyperinsulinism |
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Severe Combined Immunodeficiency, X-Linked |
|
X-Linked Severe Combined Immunodeficiency
|
SCIDX1
|
|
XSCID
|
Scidx
|
|
X-Linked Scid
|
X-Scid
|
|
Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, Nk Cell-Negative
|
Scid, X-Linked
|
|
Immunodeficiency 4
|
Imd4
|
|
Gamma Chain Deficiency
|
Scid-X1
|
|
X-Linked Combined Immunodeficiency Diseases
|
Thymic Epithelial Hypoplasia
|
|
Severe Combined Immunodeficiency T- B+ Due To Gamma Chain Deficiency
|
Severe Combined Immunodeficiency T- B+, X-Linked
|
|
Il2rg Scid, T- B+ Nk-
|
T-B+ Severe Combined Immunodeficiency Due To Gamma Chain Deficiency
|
|
T-B+ Scid Due To Gamma Chain Deficiency
|
T-B+ Severe Combined Immunodeficiency, X-Linked
|
|
Severe Combined Immunodeficiency X-Linked T-Cell-Negative/B-Cell-Positive/Nk-Cell-Negative
|
Agammaglobulinemia Swiss Type
|
|
Scid X-Linked
|
Severe Combined Immunodeficiency X-Linked T Cell-Negative/B Cell-Positive/Nk Cell-Negative
|
|
Severe Combined Immunodeficiency X-Linked T-Cell Negative/B-Cell Positive/Nk-Cell Negative
|
Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency
|
|
|
| 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
|
|
|
| Obstructive Jaundice |
|
Jaundice, Obstructive
|
Cholestatic Jaundice
|
|
Cholestatic Jaundice Syndrome
|
Obstructive Hyperbilirubinemia
|
|
Jaundice Obstructive
|
Jaundice Cholestatic
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Pituitary Gland Disease |
|
Pituitary Diseases
|
Pituitary Dysfunction
|
|
Pituitary Disease
|
Pituitary Deficiency
|
|
Pituitary Disorders
|
|
|
| Scoliosis |
|
|
| Diabetes Mellitus |
|
|
| Spondylocostal Dysostosis 1, Autosomal Recessive |
|
Jarcho-Levin Syndrome
|
SCDO1
|
|
Vertebral Anomalies
|
Spondylothoracic Dysplasia
|
|
Costovertebral Dysplasia
|
Spondylothoracic Dysostosis
|
|
Spondylocostal Dysostosis 1
|
Autosomal Recessive Spondylocostal Dysostosis 1
|
|
Spondylocostal Dysostosis, Autosomal Recessive, 1
|
Doid:0112365
|
|
Dysostosis, Spondylocostal, Autosomal Recessive, Type 1
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
