| Diseases |
Alias |
|
| Adrenal Hyperplasia, Congenital, Due To 17-Alpha-Hydroxylase Deficiency |
|
Congenital Adrenal Hyperplasia Due To 17-Alpha-Hydroxylase Deficiency
|
17-Alpha-Hydroxylase Deficiency
|
|
Deficiency Of Steroid 17-Alpha-Monooxygenase
|
Isolated 17,20-Lyase Deficiency
|
|
Adrenal Hyperplasia V
|
Congenital Adrenal Hyperplasia Type 5
|
|
17,20-Lyase Deficiency, Isolated
|
17-Alpha-Hydroxylase/17,20-Lyase Deficiency
|
|
17 Alpha-Hydroxylase/17,20-Lyase Deficiency
|
17-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia
|
|
Combined 17 Alpha-Hydroxylase/17,20-Lyase Deficiency
|
Cah Due To 17-Alpha-Hydroxylase Deficiency
|
|
Combined 17-Hydroxylase/17,20-Lyase Deficiency
|
46,Xy Disorder Of Sex Development Due To Isolated 17,20-Lyase Deficiency
|
|
17 Alpha Hydroxylase Deficiency
|
Congenital Adrenal Hyperplasia Due To 17 Alpha-Hydroxylase Deficiency
|
|
Adrenal Hyperplasia 5
|
AH5
|
|
Adrenal Hyperplasia Type V
|
Ah-V
|
|
Adrenal Hyperplasia, Congenital, Type 5
|
|
|
| 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
|
|
|
| Pseudohermaphroditism |
|
Indeterminate Sex And Pseudohermaphroditism
|
|
|
| Antley-Bixler Syndrome |
|
Trapezoidocephaly Synostosis Syndrome
|
Trapezoidocephaly-Synostosis Syndrome
|
|
Antley Bixler Syndrome
|
Multisynostotic Osteodysgenesis With Long Bone Fractures
|
|
Osteodysgenesis, Multisynostotic With Fractures
|
Antley-Bixler Syndrome, Autosomal Dominant
|
|
Antley-Bixler Syndrome Phenotype
|
|
|
| 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]
|
|
|
| Hyperandrogenism |
|
Hyperandrogenization Syndrome
|
|
|
| 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
|
|
|
| Leydig Cell Tumor |
|
Leydig Cell Neoplasm
|
Tumor, Leydig Cell
|
|
Leydig Cell Tumor, Benign
|
|
|
| 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
|
|
|
| Adrenal Adenoma |
|
Adenoma Of The Adrenal Gland
|
Adrenal Incidentaloma
|
|
Adrenal Cortical Adenoma
|
Adrenocortical Adenoma
|
|
|
| Adrenal Cortical Adenoma |
|
Adrenocortical Adenoma
|
Adenoma Adrenocortical
|
|
|
| Hypospadias |
|
Hypospadias Familial
|
Familial Hypospadias
|
|
|
| Smith-Lemli-Opitz Syndrome |
|
SLOS
|
Rsh Syndrome
|
|
7-Dehydrocholesterol Reductase Deficiency
|
Slo Syndrome
|
|
Rutledge Lethal Multiple Congenital Anomaly Syndrome
|
Lethal Acrodysgenital Syndrome
|
|
Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung
|
Smith-Opitz-Inborn Syndrome
|
|
Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobular Lung
|
Smith Lemli Opitz Syndrome
|
|
Smith-Lemli-Opitz Syndrome, Type Ii
|
|
|
| Hypokalemia |
|
Potassium Deficiency
|
Potassium Deficiency Disorder
|
|
Hypopotassemia
|
Potassium
|
|
Potassium [K] Deficiency
|
Hypokalaemic Syndrome
|
|
Hypopotassaemia
|
Hypopotassaemia Syndrome
|
|
Hypokalaemic
|
Potassium Depletion
|
|
|
| Cytochrome P450 Oxidoreductase Deficiency |
|
Por Deficiency
|
Pord
|
|
Antley-Bixler Syndrome With Disordered Steroidogenesis
|
Antley-Bixler Syndrome
|
|
Antley-Bixler Syndrome-Like Phenotype With Disordered Steroidogenesis
|
Combined Partial Deficiency Of 17-Hydroxylase And 21-Hydroxylase
|
|
Congenital Adrenal Hyperplasia Due To Apparent Combined P450c17 And P450c21 Deficiency
|
Antley-Bixler Syndrome, Autosomal Dominant
|
|
|
| Steroid Inherited Metabolic Disorder |
|
Steroid Metabolism, Inborn Errors
|
|
|
| Amenorrhea |
|
Absence Of Menstruation
|
Amenia
|
|
|
| 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
|
|
|
| Sertoli-Leydig Cell Tumor |
|
Sertoli-Leydig Cell Tumors
|
Androblastoma Of Ovary
|
|
Arrhenoblastoma
|
Arrhenoblastoma Of Ovary
|
|
Sertoli-Leydig Cell Tumor Of The Ovary
|
Sertoli-Leydig Cell Tumor Of Intermediate Differentiation
|
|
Sertoli-Leydig Cell Tumor Of Ovary
|
|
|
| Endometrial Hyperplasia |
|
|
| Adrenal Cortical Carcinoma |
|
Adrenocortical Carcinoma
|
Adrenal Cortex Carcinoma
|
|
Carcinoma Of The Adrenal Cortex
|
Acc
|
|
Adrenocortical Cancer
|
Carcinoma Adrenocortical
|
|
|
| Penis Agenesis |
|
Micropenis
|
Agenesis Of The Penis
|
|
Penis Agenesia
|
|
|
| Stuttering |
|
Stammering
|
Familial Persistent Stuttering
|
|
Stuttering, Familial Persistent 1
|
|
|
| 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
|
|
|
| Hypoadrenocorticism, Familial |
|
Addison Disease
|
Primary Adrenocortical Insufficiency
|
|
Addison'S Disease
|
Adrenal Gland Hypofunction
|
|
Adrenal Hypoplasia
|
Adrenal Aplasia
|
|
Addison Disease, Chronic Adrenal Insufficiency
|
Primary Hypoadrenalism
|
|
Hypoadrenocorticism Familial
|
Autoimmune Addison Disease
|
|
Autoimmune Adrenalitis
|
Classic Addison Disease
|
|
Primary Addison Disease
|
Addisons Disease
|
|
Addison Disease, Susceptibility To
|
Autoimmune Primary Adrenal Insufficiency
|
|
Addison'S Disease Due To Autoimmunity
|
|
|
| Leiomyoma |
|
Leiomyomatous Neoplasm
|
Leiomyomatous Tumor
|
|
Leiomyomas
|
Fibroid Tumor
|
|
Uterine Fibroids
|
|
|
| Acne |
|
Acne Vulgaris
|
Acne Varioliformis
|
|
Frontalis Acne
|
|
|
| Adrenal Carcinoma |
|
Adrenal Cancer
|
Adrenal Gland Cancer
|
|
Malignant Neoplasm Of Adrenal Gland
|
Adrenal Gland Neoplasms
|
|
Carcinoma Of The Adrenal Gland
|
Adrenal Neoplasm
|
|
Malignant Adrenal Tumor
|
Neoplasm Of Adrenal Gland
|
|
Tumor Of The Adrenal Gland
|
Adrenal Gland Neoplasm
|
|
Adrenocortical Carcinoma
|
Adrenal Gland Malignancy
|
|
Suprarenal Cancer
|
Malignant Neoplasm Of Suprarenal Gland
|
|
Malignant Neoplasm Of Adrenal Gland, Unspecified
|
Malignant Tumour Of Adrenal Gland
|
|
Suprarenal Gland Cancer
|
Primary Malignant Neoplasm Of Adrenal Gland
|
|
|
| Gender Incongruence |
|
Gender Dysphoria
|
Transsexualism
|
|
Gender Identify Disorder
|
|
|
| Mycetoma |
|
Madura Foot
|
Mycetoma Of Foot
|
|
|
| Asperger Syndrome |
|
Asperger Disorder
|
Asperger Syndrome, Susceptibility To
|
|
|
| Leydig Cell Hypoplasia |
|
46,Xy Disorder Of Sex Development Due To Lh Resistance Or Lhb Deficiency
|
46,Xy Disorder Of Sex Development Due To Luteinizing Hormone Resistance Or Luteinizing Hormone Beta Subunit Deficiency
|
|
46,Xy Dsd Due To Lh Resistance Or Lhb Deficiency
|
46,Xy Dsd Due To Luteinizing Hormone Resistance Or Luteinizing Hormone Beta Subunit Deficiency
|
|
46,Xy Disorder Of Sex Development Due To Lh Defects
|
Lh Resistance Due To Lh Receptor Deactivation
|
|
Leydig Cell Agenesis
|
Male Hypergonadotropic Hypogonadism Due To Lhcgr Defect
|
|
Male Pseudohermaphroditism Due To Lh Resistance Or Lhb Deficiency
|
Male Pseudohermaphroditism Due To Luteinizing Hormone Resistance Or Luteinizing Hormone Beta Subunit Deficiency
|
|
Lch
|
Hypoplasia, Leydig Cell
|
|
|
| Autoimmune Polyendocrine Syndrome, Type I, With Or Without Reversible Metaphyseal Dysplasia |
|
APS1
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
|
|
Apeced
|
Pga I
|
|
Hypoadrenocorticism With Hypoparathyroidism And Superficial Moniliasis
|
Autoimmune Polyendocrinopathy Syndrome , Type I, With Or Without Reversible Metaphyseal Dysplasia
|
|
Polyglandular Autoimmune Syndrome, Type 1
|
Autoimmune Polyglandular Syndrome Type 1
|
|
Autoimmune Polyendocrine Syndrome Type 1
|
Autoimmune Polyendocrinopathy Syndrome Type 1
|
|
Whitaker Syndrome
|
Aps Type 1
|
|
Polyglandular Type I Autoimmune Syndrome
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome
|
|
Aps I
|
Autoimmune Polyglandular Syndrome, Type I
|
|
Polyglandular Autoimmune Syndrome, Type I
|
Aps 1
|
|
Autoimmune Polyglandular Syndrome Type I
|
Pga 1
|
|
Pga-I
|
Polyglandular Autoimmune Syndrome Type 1
|
|
Type I Polyglandular Autoimmune Syndrome
|
Aire Deficiency
|
|
Autoimmune Polyendocrinopathy With Candidiasis And Ectodermal Dystrophy
|
Autoimmune Polyglandular Syndrome, Type 1
|
|
Autoimmune Polyendocrinopathy Type 1
|
Apeced Syndrome
|
|
Autoimmune Hypoparathyroidism-Chronic Candidiasis-Addison Disease Syndrome
|
Ham Syndrome
|
|
Hypoparathyroidism-Addison Disease-Mucocutaneous Candidiasis Syndrome
|
Medac Syndrome
|
|
Multiple Endocrine Deficiency-Addison Disease-Candidiasis Syndrome
|
Autoimmune Polyendocrine Syndrome 1, With Or Without Reversible Metaphyseal Dysplasia
|
|
Aps-1
|
Autoimmune Polyendocrine Syndrome Type I
|
|
Autoimmune Polyendocrinopathy Syndrome Type I
|
Autosomal Dominant Autoimmune Polyendocrinopathy Syndrome Type I
|
|
Polyglandular Autoimmune Syndrome Type I
|
Polyglandular Deficiency Syndrome Persian-Jewish Type
|
|
Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant
|
Polyendocrinopathy Autoimmune, Type 1, With/Without Reversible Metaphyseal Dysplasia
|
|
|
| Endometriosis |
|
Endometriosis, Site Unspecified
|
Endometrial Ectopia
|
|
|
| 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
|
|
|
| Ovarian Disease |
|
Ovarian Dysfunction
|
Ovarian Diseases
|
|
Ovarian Disorders
|
Disorder Of Endocrine Ovary
|
|
|
| Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal, Partial Or Complete |
|
P450scc Deficiency
|
Congenital Adrenal Insufficiency
|
|
Adrenal Insufficiency, Congenital, With 46xy Sex Reversal, Partial Or Complete
|
46,Xy Disorder Of Sex Development-Adrenal Insufficiency Due To Cyp11a1 Deficiency
|
|
Xy Sex Reversal-Adrenal Failure
|
Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal
|
|
AICSR
|
Adrenal Insufficiency Congenital With 46,Xy Sex Reversal Partial Or Complete
|
|
Adrenal Insufficiency, Congenital
|
Congenital Adrenal Hyperplasia
|
|
Adrenogenital Syndrome
|
|
|
| 46,Xy Sex Reversal 2 |
|
Dosage-Sensitive Sex Reversal
|
Dss
|
|
SRXY2
|
46,Xy Sex Reversal, Dax1-Related
|
|
46xy Sex Reversal 2, Dosage-Sensitive
|
46,Xy Sex Reversal Dax1-Related
|
|
|
| Hydronephrosis |
|
Stricture Of Ureteropelvic Junction With Hydronephrosis
|
Hydronephrosis With Ureteral Stricture, Not Elsewhere Classified
|
|
|
| Adrenal Gland Disease |
|
Adrenal Gland Diseases
|
Adrenal Gland Disorders
|
|
|
| Cortisone Reductase Deficiency |
|
11-Alpha Beta-Hydroxysteroid Dehydrogenase Type I Deficiency Of
|
Cortrd
|
|
Hsd 11b1 Deficiency
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Disorder Of Sexual Development |
|
Disorder Of Sex Development
|
Disorders Of Sex Development
|
|
Sex Development Disorder
|
Sex Differentiation Disease
|
|
Dsd
|
Sex Differentiation Disorders
|
|
|
| 46,Xy Sex Reversal |
|
Swyer Syndrome
|
Pure Gonadal Dysgenesis 46,Xy
|
|
Gonadal Dysgenesis, Xy Female Type
|
Gonadal Dysgenesis, 46,Xy
|
|
46,Xy Cgd
|
46,Xy Complete Gonadal Dysgenesis
|
|
46,Xy Pure Gonadal Dysgenesis
|
46 Xy Gonadal Dysgenesis
|
|
46, Xy Cgd
|
46, Xy Complete Gonadal Dysgenesis
|
|
46, Xy Pure Gonadal Dysgenesis
|
Xy Pure Gonadal Dysgenesis
|
|
Female With 46,Xy Karyotype
|
Xy Females
|
|
|
| Androgen Insensitivity, Partial |
|
Partial Androgen Insensitivity Syndrome
|
Reifenstein Syndrome
|
|
PAIS
|
Androgen Insensitivity, Partial, With Or Without Breast Cancer
|
|
Familial Incomplete Male Pseudohermaphroditism, Type 1
|
Androgen Insensitivity Syndrome, Partial
|
|
Androgen Resistance Syndrome, Partial
|
Reifenstein Syndrome, Partial
|
|
Partial Androgen Resistance Syndrome
|
Androgen Insensitivity Partial With Or Without Breast Cancer
|
|
Androgen Insensitivity Syndrome Partial
|
Insensitivity Syndrome, Androgen, Partial, With/Without Breast Cancer Syndrome
|
|
|
| Anovulation |
|
|
| Hyperaldosteronism, Familial, Type I |
|
Glucocorticoid-Remediable Aldosteronism
|
Gra
|
|
Familial Hyperaldosteronism Type 1
|
Hyperaldosteronism, Familial Type 1
|
|
HALD1
|
Fh I
|
|
Glucocorticoid-Suppressible Hyperaldosteronism
|
Gsh
|
|
Acth-Dependent Hyperaldosteronism Syndrome
|
Aldosteronism, Glucocorticoid-Remediable
|
|
Dexamethasone Sensitive Hypertension
|
Glucocorticoid Sensitive Hypertension
|
|
Familial Hyperaldosteronism Type I
|
Fh1
|
|
Aldosteronism, Sensitive To Dexamethasone
|
Dexamethasone-Sensitive Hypertension
|
|
Fh-I
|
Glucocorticoid-Sensitive Hypertension
|
|
Hyperaldosteronism, Familial, 1
|
Aldosteronism Sensitive To Dexamethasone
|
|
Familial Hyperaldosteronism 1
|
Fh Type 1
|
|
Familial Aldosteronism Type I
|
|
|
| Adrenal Cortex Disease |
|
|
| Complete Androgen Insensitivity Syndrome |
|
Cais
|
Complete Androgen Resistance Syndrome
|
|
Androgen Insensitivity Syndrome Complete
|
Androgen Insensitivity, Complete
|
|
Androgen-Insensitivity Syndrome
|
Testicular Feminization
|
|
|
| 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
|
|
|
| Ovarian Dysgenesis 2 |
|
Premature Ovarian Failure 4
|
ODG2
|
|
Ovarian Dysgenesis, Hypergonadotropic, X-Linked
|
Ovarian Failure, Hypergonadotropic, Due To Ovarian Dysgenesis
|
|
Ovarian Failure Hypergonadotropic Due To Ovarian Dysgenesis
|
X-Linked Hypergonadotropic Ovarian Dysgenesis
|
|
POF4
|
Dysgenesis, Ovarian, Type 2
|
|
|
| Transvestism |
|
Dual-Role Transvestism
|
Fetishistic Transvestism
|
|
Cross Dresser
|
Transvestic Fetishism
|
|
|
| Bronchiectasis 3 |
|
|
| Androgen Insensitivity Syndrome |
|
Androgen Resistance Syndrome
|
AIS
|
|
Testicular Feminization Syndrome
|
Androgen Receptor Deficiency
|
|
Dhtr Deficiency
|
Dihydrotestosterone Receptor Deficiency
|
|
Ar Deficiency
|
Testicular Feminization
|
|
Tfm
|
Androgen Insensitivity
|
|
Androgen-Insensitivity Syndrome
|
Goldberg-Maxwell Syndrome
|
|
Complete Androgen Insensitivity Syndrome
|
Cais
|
|
Feminisation - Testicular
|
Goldberg - Maxwell Syndrome
|
|
Androgen Insensitivity Syndrome, Complete
|
Morris Syndrome
|
|
Ary
|
AR
|
|
Insensitivity Syndrome, Androgen
|
Androgen Insensitivity Nos
|
|
|
| Sebaceous Gland Disease |
|
Sebaceous Gland Anomaly
|
Sebaceous Gland Diseases
|
|
|
| Mineral Metabolism Disease |
|
Mineral Metabolism Disorder
|
Disorder Of Mineral Metabolism
|
|
|
| Primary Pigmented Nodular Adrenocortical Disease |
|
Ppnad
|
Primary Pigmented Nodular Adrenal Dysplasia
|
|
Pigmented Nodular Adrenocortical Disease, Primary, 2
|
Pigmented Nodular Adrenocortical Disease, Primary, 1
|
|
|
| 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
|
|
|
| Familial Glucocorticoid Deficiency |
|
Glucocorticoid Deficiency
|
Acth Resistance
|
|
Adrenal Unresponsiveness To Acth
|
Hereditary Unresponsiveness To Adrenocorticotropic Hormone
|
|
Isolated Glucocorticoid Deficiency
|
Glucocorticoid Deficiency, Familial
|
|
Glucocorticoid Deficiency 1
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Osteogenesis Imperfecta, Type Xi |
|
Osteogenesis Imperfecta Type 11
|
OI11
|
|
Osteogenesis Imperfecta Type Xi
|
Oi, Type Xi
|
|
Osteogenesis Imperfecta 11
|
Oi Type Xi
|
|
Oi-Xi
|
|
|
| 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
|
|
|
| Craniosynostosis |
|
Premature Closure Of Cranial Sutures
|
Craniostenosis
|
|
Craniosynostosis Syndrome
|
Cso
|
|
Craniosynostoses
|
Congenital Ossification Of Cranial Sutures
|
|
Congenital Ossification Of Sutures Of Skull
|
Craniostosis
|
|
Imperfect Fusion Of Skull
|
Congenital Imperfect Closure Skull
|
|
Imperfect Closure Skull
|
Premature Closure Cranium Sutures
|
|
Deficiency Of Craniofacial Axis
|
|
|
