Retinitis pigmentosa Disease

About Gene:

Retinitis pigmentosa is a genetic disease that leads to the degradation of cells in the retina.

Number of Patients: 1

Disease Causing Genes:

ARL2BP RP34 RP24 RP9 RP29 PANK2 RPGRIP1 NFE2L2 MAPK8 GSN MERTK CLCC1 EYS OFD1 EXOSC2 CC2D2A ZNF408 CYP4V2 BBS1 NPHP4 TUB GDPD1 Rdh12 DFCTRPS RPY PROM1 NEK2 CNGB1 RGR PCARE PLIN2 KIZ GUCA1A MKKS WDR19 GUCA1C Znf513 POMGNT1 ABCA4 ARL6 SAMD11 FSCN2 AHR IMPDH1 CERKL GUCY2D RHO ROM1 LRAT IDH3B GUCA1B AGBL5 SLC7A14 TTPA BBS4 TENT5A MPP4 CLN3 SAG HK1 RBP4 DHX38 HKDC1 TTC8 IFT43 CNGB3 RCVRN ENSA RRH TOPORS ABHD12 USH2A NR2E3 SEMA4A BBS2 RDH11 GNB1 RCC1 ADGRV1 SPATA7 RCBTB1 YPEL2 TUT1 PRPF31 PDE6G PRPF6 HGSNAT CHM FLVCR1 LPCAT1 USH1C PDC BCAN WDR17 GUCY2F BEST1 PDE6B PRPF4 KIF3B IFT172 GGCX PRCD C5AR2 RIMS1 IMPG1 ARSI RPGR CNGA1 EDN1 RP9P IFT140 KIAA1549 CACNA1F RLBP1 RPGRIP1L RAX2 SLC24A1 SAMD7 RPE65 PRPF8 PRPF3 LOC100421404 IMPG2 TPX2 TNPO1 NMNAT1 GRK1 CEP78 EML1 ATP6 RP1 PRPH2 AIPL1 TIMP3 IDH3A REEP6 MVK AHI1 PEX6 INVS CWC27 RP2 RBP3 CFH TRNT1 ADIPOR1 ARHGEF18 SMC3 MFRP IQCB1 DACT2 COL6A6 Crb1 PDE6A CLRN1 TULP1 KLHL7 CANX PRKCG PRPS1 RDH5 MDH1 CDHR1 OR2W3 Rp22 RP1L1 SNRNP200 CRX DHDDS CFAP418 SMC1A CA4 ELOVL4 UXT CRB2 NXNL1 Rp6 FAM161A RP63 NRL MAK GLO1 SCAPER CDH23 VPS13B CEP250 LCA5 KATNIP Arl3

Sign and Symptoms:

  1. Blindness

Diagnosis:

(1) Medical history collection (2) Neurological examination (3) Fundoscopy

Preventions:

Treatment:

Low vison aids vision rehabilitation