OMIA:001661-9615 : Adrenal hyperplasia, congenital, due to 11-beta hydroxylase deficiency in Canis lupus familiaris (dog) |
In other species: domestic cat
Categories: Endocrine / exocrine gland phene (incl mammary gland)
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 202010 (trait) , 610613 (gene)
Links to MONDO diseases:
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: This is a type of XX difference of sexual development (DSD) due to variants in the CYP11B1 gene.
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:001661-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Edit History
- Created by Imke Tammen2 on 31 May 2023