| Symbol
| MCDR1
|
| Location
| 6q16.2
|
| HGNC id
| 6939
|
| Name
|
macular dystrophy, retinal 1, North Carolina type |
| Other name(s)
|
central areolor pigment epithelial dystrophy
foveal dystrophy, progressive
retinal pigment epithelial dystrophy, central |
| Corresponding gene
|
PRDM13
|
| related resource
| Retinal Information Network
|
| Other symbol(s)
| CAPED, NCMD
|
| Main clinical features
|
progressive bifocal chorioretinal atrophy, Belize macular dystrophy |
| Genetic determination
| autosomal dominant |
| Related entries
| including autosomal dominant drusen and atrophic macular degeneration
|
| Function/system disorder
| eye |
| Type
| disease
|