All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03582 HPMRS-3;GPIBD-8 hyperphosphatasia, with mental retardation syndrome, type 3 (HPMRS-3, glycosylphosphatidylinositol deficiency, type 8 (GPIBD-8)) 614207 - 12 11 PGAP2 - autosomal recessive
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