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Disease Ontology Browser
primary hyperoxaluria type 3 (DOID:0111672)
Alliance: disease page
Synonyms: HP3; PH III; primary hyperoxaluria type III
Alt IDs: OMIM:613616, NCI:C123214, ORDO:93600, UMLS_CUI:C3150878
Definition: A primary hyperoxaluria characterized by recurring calcium oxalate stones that has_material_basis_in homozygous or compound heterozygous mutation in the HOGA1 gene on chromosome 10q24.2.

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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12/10/2024
MGI 6.24 		The Jackson Laboratory