All individuals with variants in gene WDPCP

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

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00144158 - PubMed: Katagiri 2014 index patient M no Japan Japanese - - - - retinal disease - 1 1 Rob W.J. Collin
00292799 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00380364 - PubMed: M'hamdi_2014 - F yes Tunisia Tunisian - - - - retinal disease retinitis pigmentaria 1 1 LOVD
00385232 - PubMed: Redin-2012 - - - France - - - - - retinal disease - 1 1 LOVD
00385285 - PubMed: M'hamdi-2014 - F yes Tunisia Tunisian - - - - retinal disease obesity, retinitis pigmentosa, polydactyly, hypogenitalism,mental retardation 1 1 LOVD
00386873 121-024 PubMed: Zampaglione 2020 - ? - - - - - - - retinal disease - 1 1 LOVD
00386885 OGI1165_002272 PubMed: Zampaglione 2020 - ? - - - - - - - retinal disease - 1 1 LOVD
00395608 RP-2966 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease cone/cone-rod dystrophy, myopia, oligomenorrhea, global developmental delay, intellectual disability, polydactyly 1 1 LOVD
00417830 AR248 PubMed: Kim 2010 - M - - - - - - - BBS - 1 1 LOVD
00417831 AR316 PubMed: Kim 2010 - ? - - - - - - - BBS - 1 1 LOVD
00417832 MR-1 PubMed: Kim 2010 - ? - - - - - - - BBS - 1 1 LOVD
00417833 MKS142 PubMed: Kim 2010 - ? - - - - - - - retinal disease - 1 1 LOVD
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