| Diseases |
Alias |
|
| Adrenal Hyperplasia, Congenital, Due To Steroid 11-Beta-Hydroxylase Deficiency |
|
Congenital Adrenal Hyperplasia Due To 11-Beta-Hydroxylase Deficiency
|
11-Beta-Hydroxylase Deficiency
|
|
P450c11b1 Deficiency
|
Deficiency Of Steroid 11-Beta-Monooxygenase
|
|
Adrenal Hyperplasia Iv
|
Steroid 11-Beta-Hydroxylase Deficiency
|
|
Adrenal Hyperplasia, Hypertensive Form
|
Adrenal Hyperplasia, Congenital, Due To 11-Beta-Hydroxylase Deficiency
|
|
Adrenal Hyperplasia 4
|
Cah Due To 11-Beta-Hydroxylase Deficiency
|
|
Cyp11b1 Deficiency
|
11 Beta Hydroxylase Deficiency
|
|
Adrenal Hyperplasia Hypertensive Form
|
11b Hydroxylase Deficiency
|
|
Steroid 11 Beta Hydroxylase Deficiency
|
AH4
|
|
Adrenal Hyperplasia Type Iv
|
Ah-Iv
|
|
Steroid 11-Beta-Monooxygenase Deficiency
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Adrenal Adenoma |
|
Adenoma Of The Adrenal Gland
|
Adrenal Incidentaloma
|
|
Adrenal Cortical Adenoma
|
Adrenocortical Adenoma
|
|
|
| Adrenal Cortical Adenoma |
|
Adrenocortical Adenoma
|
Adenoma Adrenocortical
|
|
|
| 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
|
|
|
| Steroid Inherited Metabolic Disorder |
|
Steroid Metabolism, Inborn Errors
|
|
|
| Adenoma |
|
Acinar Cell Adenoma
|
Adenomas
|
|
Acinic Cell Adenoma
|
|
|
| Corticosterone Methyloxidase Type I Deficiency |
|
Cmo I Deficiency
|
Aldosterone Deficiency I
|
|
Aldosterone Deficiency Due To Defect In Steroid 18-Hydroxylase
|
18-Hydroxylase Deficiency
|
|
Hypoaldosteronism, Congenital, Due To Cmo I Deficiency
|
Corticosterone Methyloxidase Deficiency 1
|
|
Corticosterone Methyloxidase Type 1 Deficiency
|
Hyperreninemic Hypoaldosteronism, Familial, 1
|
|
Fhha1a
|
Steroid 18-Hydroxylase Deficiency
|
|
Aldosterone Synthase Deficiency
|
18 Hydroxylase Deficiency
|
|
18 Alpha Hydroxylase Deficiency
|
Aldosterone Deficiency 1
|
|
Aldosterone Deficiency Due To Defect In 18 Hydroxylase
|
Cmo 1 Deficiency
|
|
Corticosterone Methyloxidase 1 Deficiency
|
CMO-1 DEFICIENCY
|
|
Aldosterone Deficiency Due To Defect In 18-Hydroxylase
|
Corticosterone Methyl Oxidase Type I Deficiency
|
|
Corticosterone Methyl Oxidase Type Ii Deficiency
|
|
|
| Hypokalemia |
|
Potassium Deficiency
|
Potassium Deficiency Disorder
|
|
Hypopotassemia
|
Potassium
|
|
Potassium [K] Deficiency
|
Hypokalaemic Syndrome
|
|
Hypopotassaemia
|
Hypopotassaemia Syndrome
|
|
Hypokalaemic
|
Potassium Depletion
|
|
|
| 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
|
|
|
| Adrenal Gland Disease |
|
Adrenal Gland Diseases
|
Adrenal Gland Disorders
|
|
|
| Adrenal Rest Tumor |
|
|
| Asperger Syndrome |
|
Asperger Disorder
|
Asperger Syndrome, Susceptibility To
|
|
|
| Adrenal Cortical Carcinoma |
|
Adrenocortical Carcinoma
|
Adrenal Cortex Carcinoma
|
|
Carcinoma Of The Adrenal Cortex
|
Acc
|
|
Adrenocortical Cancer
|
Carcinoma Adrenocortical
|
|
|
| Apparent Mineralocorticoid Excess |
|
Cortisol 11-Beta-Ketoreductase Deficiency
|
Apparent Mineralocorticoid Excess Syndrome
|
|
AME
|
Ame1
|
|
11-Beta-Hydroxysteroid Dehydrogenase Deficiency Type 2
|
Ulick Syndrome
|
|
Mineralocorticoid Excess Syndrome, Apparent
|
Syndrome Of Apparent Mineralocorticoid Excess
|
|
Ame 1
|
11 Beta Hydroxysteroid Dehydrogenase Type 2 Deficiency
|
|
|
| Adrenal Cortex Disease |
|
|
| 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
|
|
|
| 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
|
|
|
| Acth-Independent Macronodular Adrenal Hyperplasia |
|
Acth-Independent Macronodular Adrenocortical Hyperplasia
|
Adrenocorticotropic Hormone-Independent Macronodular Adrenal Hyperplasia
|
|
Corticotropin-Independent Macronodular Adrenal Hyperplasia
|
Cushing Syndrome Due To Macronodular Adrenal Hyperplasia
|
|
AIMAH1
|
Aimah
|
|
Massive Macronodular Adrenocortical Disease
|
Mmad
|
|
Primary Macronodular Adrenal Hyperplasia
|
Cushing Syndrome, Adrenal, Due To Aimah
|
|
Primary Bilateral Macronodular Adrenal Hyperplasia
|
Acth-Independent Macronodular Adrenal Hyperplasia 1
|
|
Acth-Independent Cushing Syndrome
|
Adrenal Cushing Syndrome Due To Aimah
|
|
Acth-Independent Macronodular Adrenal Hyperplasia 2
|
|
|
| Cortisone Reductase Deficiency |
|
11-Alpha Beta-Hydroxysteroid Dehydrogenase Type I Deficiency Of
|
Cortrd
|
|
Hsd 11b1 Deficiency
|
|
|
| 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
|
|
|
| Lobomycosis |
|
Cutaneous Blastomycosis
|
Cutaneous Lobomycosis
|
|
Infection By Loboa Loboi
|
Lobo Disease
|
|
|
| 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
|
|
|
| Primary Pigmented Nodular Adrenocortical Disease |
|
Ppnad
|
Primary Pigmented Nodular Adrenal Dysplasia
|
|
Pigmented Nodular Adrenocortical Disease, Primary, 2
|
Pigmented Nodular Adrenocortical Disease, Primary, 1
|
|
|
| Liddle Syndrome 1 |
|
Liddle Syndrome
|
Pseudoaldosteronism
|
|
Liddle'S Syndrome
|
LIDLS1
|
|
Lidls
|
Pseudohyperaldosteronism
|
|
Pseudoprimary Hyperaldosteronism
|
Pseudohyperaldosteronism Type 1
|
|
Liddles Syndrome
|
|
|
| 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
|
|
|
| Endocrine Organ Benign Neoplasm |
|
|
| Carney Complex Variant |
|
Carney Complex
|
Carney Syndrome
|
|
Carney Complex, Type 1
|
Lamb Syndrome
|
|
Name Syndrome
|
Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome
|
|
Carney Complex - Trismus - Pseudocamptodactyly Syndrome
|
Carney Complex, Type 2
|
|
Car
|
Cnc1
|
|
Carney Myxoma-Endocrine Complex
|
Myxoma - Spotty Pigmentation - Endocrine Overactivity
|
|
Myxoma, Spotty Pigmentation, And Endocrine Overactivity
|
Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
|
|
Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
|
Carney Complex-Trismus-Pseudocamptodactyly Syndrome
|
|
CACOV
|
|
|
| Pseudohermaphroditism |
|
Indeterminate Sex And Pseudohermaphroditism
|
|
|
| Disorder Of Sexual Development |
|
Disorder Of Sex Development
|
Disorders Of Sex Development
|
|
Sex Development Disorder
|
Sex Differentiation Disease
|
|
Dsd
|
Sex Differentiation Disorders
|
|
|
| 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
|
|
|
