All individuals with variants in gene NECAP1

2 entries on 1 page. Showing entries 1 - 2.
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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     
00361573 11DG1144 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; global developmental delay with severe epileptic encephalopathy 1 1 Johan den Dunnen
00415261 16 PubMed: Alfares 2018 - F - - - - - - - retinal disease OMIM: 615833; developmental delay, hypotonia, and seizure disorder 1 1 LOVD
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