Disease #00326 (MCOP8 (microphthalmia, isolated, type 8 (MCOP-8)), OMIM:615113)
| Official abbreviation |
MCOP8 |
| Name |
microphthalmia, isolated, type 8 (MCOP-8) |
| OMIM ID |
615113 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
ALDH1A3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-02-16 17:01:25 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|