All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04087 MRT-42;GPIBD-9 mental retardation, autosomal recessive, type 42 (MRT-42, glycosylphosphatidylinositol deficiency, type 9 (GPIBD-9)) 615802 3 3 PGAP1 - autosomal recessive