congenital adrenal hyperplasia

Summary
Synonym
  • adrenal hyperplasia 1
  • congenital lipoid adrenal hyperplasia
  • lipoid CAH
Definition
A steroid inherited metabolic disorder that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgeny manifestations resulting from steroidogenic enzyme deficiency.
Super Class
physical disorder steroid inherited metabolic disorder
External Links
Disease Ontology
DOID:0050811
Mondo Disease Ontology
UMLS
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 26 of 26 in total
Gene ID Gene Symbol Description Source
4191 MDH2 malate dehydrogenase 2
6390 SDHB succinate dehydrogenase complex iron sulfur subunit B
8630 HSD17B6 hydroxysteroid 17-beta dehydrogenase 6
9469 CHST3 carbohydrate sulfotransferase 3
55997 CFC1 cryptic, EGF-CFC family member 1
146183 OTOA otoancorin
The Human Phenotype Ontology
Displaying entries 61 - 70 of 100 in total
HPO ID HPO Term
HP:0008258 Congenital adrenal hyperplasia
HP:0008675 Enlarged polycystic ovaries
HP:0008689 Bilateral cryptorchidism
HP:0008726 Hypoplasia of the vagina
HP:0008730 Female external genitalia in individual with 46,XY karyotype
HP:0008734 Decreased testicular size
HP:0010465 Precocious puberty in females
HP:0011749 Adrenocorticotropic hormone excess
HP:0011969 Elevated circulating luteinizing hormone level
HP:0012041 Decreased fertility in males
Displaying all 4 entries
Gene ID Gene Symbol Description
1586 CYP17A1 cytochrome P450 family 17 subfamily A member 1
3284 HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
1584 CYP11B1 cytochrome P450 family 11 subfamily B member 1
1589 CYP21A2 cytochrome P450 family 21 subfamily A member 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024