All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05403 MRT53;GPIBD13 mental retardation, autosomal recessive, type 53 (MRT-53, glycosylphosphatidylinositol deficiency, type 13 (GPIBD-13)) 616917 AR 1 1 PIGG - autosomal recessive
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