All individuals with variants in gene SPTBN1

3 entries on 1 page. Showing entries 1 - 3.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00405008 - - - M yes Egypt - - - - - SCA5 27-y male The patient presents with abnormality of movement, ataxia, fasciculations, muscle weakness, muscular hypotonia, peripheral neuropathy, skeletal muscle atrophy and tremor. 1 1 Sherifa Ahmed Hamed
00451701 - - - M - - (not applicable) white - - - - NDD HP:0001263, HP:0001290, HP:0001382, HP:0000286, HP:0000268, HP:0000494, HP:0000307, HP:0100021, HP:0001264, HP:0001622, HP:0100651 1 1 Marketa Wayhelova
00466851 - - - M - - (not applicable) - - - - - NDD HP:0001256, HP:0002342, HP:0000729, HP:0001252, HP:0002487 1 1 Marketa Wayhelova
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