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
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