Disease #02903 (MCOPS5 (microphthalmia, syndromic, type 5 (dystrophy, retinal, early onset)), OMIM:610125)
| Official abbreviation |
MCOPS5 |
| Name |
microphthalmia, syndromic, type 5 (dystrophy, retinal, early onset) |
| OMIM ID |
610125 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
OTX2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-12-23 15:02:48 +01:00 (CET) |
Individuals
|