All individuals with variants in gene VIM

9 entries on 1 page. Showing entries 1 - 9.
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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     
00013434 - - - F - Germany - - - no (pedigree) - FAP1 no additional phenotype data available; colorectal phenotype classical, ? nr polyps 1 1 Stefan Aretz
00059928 - - 45y female patient F - - DE - - - - CTRCT pulverent cataract 1 1 Ivo F.A.C. Fokkema
00290017 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 21 Mohammed Faruq
00385514 17004217 PubMed: Lenassi 2020 retrospective analysis M - (United Kingdom (Great Britain)) - - - - - retinal disease - 1 1 LOVD
00434036 Fam14 PubMed: Zhai 2017 4-generation family, 3 affected (3M) M - China - - - - - CTRCT posterior polar cataract 1 3 Johan den Dunnen
00444908 Fam25PatII1 PubMed: Ma 2016 2-generation family, 1 affected, unaffected parents M - Australia - - - - - CTRCT see paper; ..., bilateral cataract, 1y-visual acuity 6/36 bilateral 1 1 Johan den Dunnen
00445070 CC0000553 PubMed: Kessel 2021 patient - - Denmark - - - - - CTRCT cataract 1 1 Johan den Dunnen
00446498 Fam105Pat286 PubMed: Liu 2023 2-generation family, affected mother/daughter F - China - - - - - CTRCT bilateral congenital cataract 1 2 Johan den Dunnen
00446499 Fam105Pat287 PubMed: Liu 2023 mother F - China - - - - - CTRCT bilateral congenital cataract 1 1 Johan den Dunnen
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