Disease #04519 (VMD5 (dystrophy, macular, vitelliform, type 5 (VMD-5)), OMIM:616152)
| Official abbreviation |
VMD5 |
| Name |
dystrophy, macular, vitelliform, type 5 (VMD-5) |
| OMIM ID |
616152 |
| 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 |
IMPG2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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