Disease #03413 (adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete, OMIM:613743)
| Official abbreviation |
- |
| Name |
adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete |
| OMIM ID |
613743 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
CYP11A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-10-03 10:44:38 +02:00 (CEST) |
Individuals
|