hyperphosphatasia with impaired intellectual development syndrome 3

Summary

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: glycosylphosphatidylinositol biosynthesis defect 8, GPIBD8, HPMRS3, hyperphosphatasia with mental retardation syndrome 3

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: pgap2

MIM:

MIM:614207 - HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 3; HPMRS3

MIM:614207 - HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 3; HPMRS3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): hyperphosphatasia with impaired intellectual development syndrome (is_a)