Disease #00030 (CAH1 (ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY), OMIM:201910)
| Official abbreviation |
CAH1 |
| Name |
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY |
| OMIM ID |
201910 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CYP21A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-07-11 10:01:21 +00:00 (UTC) |
| Date last edited |
2023-06-16 09:08:48 +00:00 (UTC) |
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