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Disease Ontology Browser
congenital adrenal hyperplasia (DOID:0050811)
Alliance: disease page
Synonyms: adrenal hyperplasia 1; congenital lipoid adrenal hyperplasia; lipoid CAH
Alt IDs: OMIM:201710, OMIM:201810, OMIM:201910, OMIM:202010, OMIM:202110, ICD10CM:E25, ICD10CM:E25.9, ICD9CM:255.2, ORDO:418, UMLS_CUI:C0701163
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.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/01/2019
MGI 6.14
The Jackson Laboratory