Disease #01632 (GCCD1 (glucocorticoid deficiency, due to ACTH unresponsiveness (GCCD1, ACTH resistance)), OMIM:202200)
| Official abbreviation |
GCCD1 |
| Name |
glucocorticoid deficiency, due to ACTH unresponsiveness (GCCD1, ACTH resistance) |
| OMIM ID |
202200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
MC2R |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-11-02 11:38:34 +01:00 (CET) |
Individuals
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