OMIA:002948 : Adrenal hyperplasia, congenital, CYP21A2-related |
Categories: Endocrine / exocrine gland phene (incl mammary gland)
Possible human homologues (MIM numbers): 613815 (gene) , 201910 (trait)
Cross-species summary: 21-hydroxylase deficiency in humans causes congenital adrenal hyperplasia and nonclassical hyperandrogenism.
Species in which this phene is found:
Japanese medaka (Oryzias latipes)
Edit History
- Created by Imke Tammen2 on 30 Apr 2025
- Changed by Imke Tammen2 on 30 Apr 2025