Disease #00002 (RP (XL) (Retinitis Pigmentosa (X-linked)))
Official abbreviation |
RP (XL) |
Name |
Retinitis Pigmentosa (X-linked) |
OMIM ID |
- |
Inheritance |
X-linked |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
0 |
Associated with 7 genes |
CHM, GPR143, MED12, OFD1, RP2, RPGR, RS1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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