Disease #00186 (MCOPS2 (microphthalmia, syndromic, type 2), OMIM:300166)
| Official abbreviation |
MCOPS2 |
| Name |
microphthalmia, syndromic, type 2 |
| OMIM ID |
300166 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
BCOR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-09-05 15:25:12 +02:00 (CEST) |
| Date last edited |
2023-12-28 13:54:22 +01:00 (CET) |
Individuals
|