About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency
OMIM ID: 201910
Synonyms 21-hydroxylase Deficiency; Adrenal Hyperplasia; Adrenal Hyperplasia III; CYP21 Deficiency
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Cyp21a1 CYP21A2*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
08/26/2014
MGI 5.19
The Jackson Laboratory