Human genes for primary hyperoxaluria type 3
Primary hyperoxaluria type 3 [DOID:0111672]
A primary hyperoxaluria characterized by recurring calcium oxalate stones that has_material_basis_in homozygous or compound heterozygous mutation in HOGA1 on chromosome 10q24.2.
Synonyms: primary hyperoxaluria type 3, DOID:0111672, HP3, PH III, primary hyperoxaluria type III ...