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

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

Lab-ID     

Reference     

Remarks     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00000016 RP-17 - - RP (XL) - RP2 RP2 1 1 variome.ir
00000080 RP-95 - - RP (XL) - RS1 RS1 1 1 variome.ir
Legend   How to query