All individuals with variants in gene KCNC1

2 entries on 1 page. Showing entries 1 - 2.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00081422 - - - M no - North Africa - - - - MRT delayed motor milestones, speech delay, hypotonia, lability of attention, intellectual disability, dysmorphic features 1 1 Thierry Bienvenu
00089106 28145425-Fam PubMed: Poirier 2017, Journal: Poirier 2017 2-generation family, 3 affecteds, father, daugther and son F;M ? France - - - - - ID delayed motor milestones, speech delay, hypotonia, lability of attention, intellectual disability, normal head circumference, minor dysmorphic features incl. epicanthal folds, ptosis, short philtrum, prognathism, fetal pads, protruding ears; intellectual disability (HP:0001249); speech delay (HP:0000750) 1 3 Karine Poirier
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