All individuals with variants in gene PRG4

13 entries on 1 page. Showing entries 1 - 13.
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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     
00106541 - - - - - - - - - - - CACP - 1 1 Saliha Yilmaz
00106542 - - - - - - - - - - - CACP - 1 1 Saliha Yilmaz
00106544 - - - - yes - - - - - - CACP - 1 1 Saliha Yilmaz
00106545 - - - F yes - - - - - - CACP - 1 2 Saliha Yilmaz
00106546 - - - F yes - - - - - - CACP - 1 1 Saliha Yilmaz
00106547 - - - - - - - - - - - CACP - 2 2 Saliha Yilmaz
00106548 - - - M yes - - - - - - CACP - 1 1 Saliha Yilmaz
00106549 - - - M - - - - - - - CACP - 1 1 Saliha Yilmaz
00106550 - - - - yes - - - - - - CACP - 1 1 Saliha Yilmaz
00106551 - - - ? - - - - - - - CACP - 1 3 Saliha Yilmaz
00106552 - - - M yes - - - - - - CACP - 2 1 Saliha Yilmaz
00415253 8 PubMed: Alfares 2018 - M - - - - - - - retinal disease OMIM: 208250; multiple joint flexion deformity 1 1 LOVD
00472227 - Verebi et al. (submitted) - M - France - - - - - CACP Arthrogryposis multiplex congenita 2 1 Camille Verebi
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