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DOID:0070432 - hyperphosphatasia with impaired intellectual development syndrome 5
Disease Ontology Definition:A hyperphosphatasia with impaired intellectual development syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PIGW gene on chromosome 17q12.
Synonyms: GPIBD11, HPMRS5, glycosylphosphatidylinositol biosynthesis defect 11, hyperphosphatasia with mental retardation syndrome 5,
Xenbase Genes : pigw
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee