Disease #00003 (RP (AD) (Retinitis Pigmentosa (AD)))
Official abbreviation |
RP (AD) |
Name |
Retinitis Pigmentosa (AD) |
OMIM ID |
- |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
12 |
Phenotype entries for this disease |
0 |
Associated with 20 genes |
BBS1, BEST1, CRX, DMPK, FSCN2, GUCA1A, IMPDH1, IMPG2, KIF21A, LCA5, MFN2, PRCD, PRPF3, PRPF6, RDH12, RHO, SEMA4A, TGFBI, USH2A, ZNF423 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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