Disease #02245 (MCOPS-1 (microphthalmia, syndromic, type 1 (MCOPS-1, Lenz microphthalmia syndrome)), OMIM:309800)
| Official abbreviation |
MCOPS-1 |
| Name |
microphthalmia, syndromic, type 1 (MCOPS-1, Lenz microphthalmia syndrome) |
| OMIM ID |
309800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
BCOR, NAA10 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
