Disease #03059 (VMD2 (dystrophy, macular, vitelliform, type 2 (VMD-2 (Best macular dystrophy (BMD))), OMIM:153700)
| Official abbreviation |
VMD2 |
| Name |
dystrophy, macular, vitelliform, type 2 (VMD-2 (Best macular dystrophy (BMD)) |
| OMIM ID |
153700 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
BEST1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-04-30 09:01:13 +02:00 (CEST) |
Individuals
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