hypophosphatasia Disease Ontology Browser

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Disease Ontology Browser

hypophosphatasia (DOID:14213)
Alliance: disease page
Synonyms: deficiency of alkaline phosphatase
Alt IDs: DOID:14763, ICD10CM:E83.39, MESH:C562440, MESH:D007014, NCI:C26798, ORDO:436, UMLS_CUI:C0020630, UMLS_CUI:C0220743
Definition: A syndrome characterized by disruption of mineralization of bones and teeth that has_material_basis_in mutation in the ALPL gene on chromosome 1p36.12.

Disease References using Mouse Models (9)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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