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

12 entries on 1 page. Showing entries 1 - 12.
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AscendingIndividual ID     

Lab-ID     

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Remarks     

Disease     

Phenotype details     

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Variants in genes

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00000003 RP-3 - - RP (AD) - GUCA1A GUCA1A 1 1 variome.ir
00000004 RP-4 - - RP (AD) - CRX CRX 1 1 variome.ir
00000005 RP-5 - - RP (AD), RP (AR) - OPA1 OPA1 1 1 variome.ir
00000012 RP-10 - - RP (AD) - DMPK - 1 1 variome.ir
00000025 RP-25 - - RP (AD) - GUCY2D - 0 1 variome.ir
00000031 RP-31 - - RP (AD) - BEST1 BEST1 1 1 variome.ir
00000057 RP-61 - - RP (AD) - PRPF8 - 0 1 variome.ir
00000074 RP-83 - - RP (AD) - GUCY2D - 0 1 variome.ir
00000076 RP-88 - - RP (AD) - IMPG2 IMPG2 1 1 variome.ir
00000081 RP-96 - - RP (AD) - PRPF3 PRPF3 1 1 variome.ir
00000084 RP-99 - - RP (AD) - IMPDH1 IMPDH1 1 1 variome.ir
00000088 RP-106 - - RP (AD) - GUCY2D - 0 1 variome.ir
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