All individuals with variants in gene PIP5K1A

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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     
00361507 13DG1764 PubMed: Anazi 2017 simplex case M yes Saudi Arabia - - - - - ID syndromic; global developmental delay, dysmorphism, short stature and delayed puberty 1 1 Johan den Dunnen
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