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
|