Disease #01637 (corticosterone methyloxidase type 1 deficiency, OMIM:203400)
| Official abbreviation |
- |
| Name |
corticosterone methyloxidase type 1 deficiency |
| OMIM ID |
203400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CYP11B2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-06-15 10:15:14 +02:00 (CEST) |
Individuals
|