Adrenal Hyperplasia, Congenital [kongenitální adrenální hyperplazie]

topical
226
Terms

CAH
deficit 21-hydroxylázy
nadledviny - hyperplazie kongenitální
vrozená adrenální hyperplazie

 

Congenital Adrenal Hyperplasia
Hyperplasia, Congenital Adrenal

Persistent link   https://www.medvik.cz/link/D000312
Definition

A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders.

DUI
D000312 MeSH Browser
CUI
M0000487
History note
80; was ADRENOGENITAL SYNDROME 1963-79
Online note
use ADRENAL HYPERPLASIA, CONGENITAL to search ADRENOGENITAL SYNDROME 1966-79
Public note
80; was ADRENOGENITAL SYNDROME 1963-79

Allowable subheadings

BL
blood 11
CF
cerebrospinal fluid
CI
chemically induced 1
CL
classification 5
CO
complications 15
DI
diagnosis 110
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 25
EC
economics
EM
embryology
EN
enzymology 5
EP
epidemiology 15
EH
ethnology
ET
etiology 21
GE
genetics 50
HI
history 1
IM
immunology
ME
metabolism 4
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 11
PP
physiopathology 15
PC
prevention & control 3
PX
psychology 1
RT
radiotherapy
RH
rehabilitation
SU
surgery 15
TH
therapy 43
UR
urine 2
VE
veterinary
VI
virology

C Diseases
C12 Urogenital Diseases 8
C12.050 Female Urogenital Diseases and Pregnancy Complications 132
C12.050.351 Female Urogenital Diseases 153
C12.050.351.875 Urogenital Abnormalities 146
C12.050.351.875.253 Disorders of Sex Development 232
C12.050.351.875.253.090 Adrenogenital Syndrome 50
C12.050.351.875.253.090.500 Adrenal Hyperplasia, Congenital 226
C12.050.351.875.253.090.750 Hyperandrogenism 107
C12.200 Male Urogenital Diseases 200
C12.200.706 Urogenital Abnormalities 146
C12.200.706.316 Disorders of Sex Development 232
C12.200.706.316.090 Adrenogenital Syndrome 50
C12.200.706.316.090.500 Adrenal Hyperplasia, Congenital 226
C12.200.706.316.090.750 Hyperandrogenism 107
C12.800 Urogenital Abnormalities 146
C12.800.316 Disorders of Sex Development 232
C12.800.316.090 Adrenogenital Syndrome 50
C12.800.316.090.500 Adrenal Hyperplasia, Congenital 226
C12.800.316.090.750 Hyperandrogenism 107
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.939 Urogenital Abnormalities 146
C16.131.939.316 Disorders of Sex Development 232
C16.131.939.316.129 Adrenogenital Syndrome 50
C16.131.939.316.129.500 Adrenal Hyperplasia, Congenital 226
C16.131.939.316.129.750 Hyperandrogenism 107
C16.320 Genetic Diseases, Inborn 1 215
C16.320.033 Adrenal Hyperplasia, Congenital 226
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 86
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 48
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 58
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 47
C16.320.400 Heredodegenerative Disorders, Nervous System 46
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 6
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 714
C16.320.565.925 Steroid Metabolism, Inborn Errors 7
C16.320.565.925.249 Adrenal Hyperplasia, Congenital 226
C16.320.565.925.324 Antley-Bixler Syndrome Phenotype 1
C16.320.565.925.400 Ichthyosis, X-Linked 9
C16.320.565.925.500 Mineralocorticoid Excess Syndrome, Apparent 2
C16.320.565.925.875 Smith-Lemli-Opitz Syndrome 30
C16.320.577 Muscular Dystrophies 141
C16.320.590 Myasthenic Syndromes, Congenital 21
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 125
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 200
C18.452.648 Metabolism, Inborn Errors 714
C18.452.648.925 Steroid Metabolism, Inborn Errors 7
C18.452.648.925.249 Adrenal Hyperplasia, Congenital 226
C18.452.648.925.324 Antley-Bixler Syndrome Phenotype 1
C18.452.648.925.400 Ichthyosis, X-Linked 9
C18.452.648.925.500 Mineralocorticoid Excess Syndrome, Apparent 2
C18.452.648.925.875 Smith-Lemli-Opitz Syndrome 30
C19 Endocrine System Diseases 887
C19.053 Adrenal Gland Diseases 115
C19.053.098 Adrenal Cortex Diseases 32
C19.053.347 Adrenal Gland Neoplasms 289
C19.053.440 Adrenal Hyperplasia, Congenital 226
C19.053.500 Adrenal Insufficiency 113
C19.053.800 Adrenocortical Hyperfunction 48
C19.391 Gonadal Disorders 40
C19.391.119 Disorders of Sex Development 232
C19.391.119.090 Adrenogenital Syndrome 50
C19.391.119.090.500 Adrenal Hyperplasia, Congenital 226
C19.391.119.090.750 Hyperandrogenism 107

17,20-Lyase Deficiency, Isolated Disease MeSH Browser

Adrenal Hypoplasia, Congenital, with Precocious Puberty Disease MeSH Browser

Adrenal hyperplasia 2 Disease MeSH Browser

Adrenal hyperplasia, congenital, type 5 Disease MeSH Browser

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Disease MeSH Browser

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Disease MeSH Browser

Lipoid congenital adrenal hyperplasia Disease MeSH Browser

Mineralocorticoid Deficiency, Isolated Disease MeSH Browser

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