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DOID:0070435 - hyperphosphatasia with impaired intellectual development syndrome 3
Disease Ontology Definition:A hyperphosphatasia with impaired intellectual development syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PGAP2 gene on chromosome 11p15.
Synonyms: GPIBD8, HPMRS3, glycosylphosphatidylinositol biosynthesis defect 8, hyperphosphatasia with mental retardation syndrome 3,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee