Disease #00112 (CAH (Congenital Adrenal Hyperplasia), OMIM:201910)
Official abbreviation |
CAH |
Name |
Congenital Adrenal Hyperplasia |
OMIM ID |
201910 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
CYP21A2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|