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| Term | primary hyperoxaluria type 3 | ID (Ontology) | DOID:0111672 (Human Disease) |
| 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. | ||
| Also Known As | "HP3" ; "PH III" ; "primary hyperoxaluria type III" | ||
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carbohydrate metabolic disorder |__primary hyperoxaluria |__primary hyperoxaluria type 3 |
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| Is a | primary hyperoxaluria | ||
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GARD:10738 MIM:613616 NCI:C123214 ORDO:93600 SNOMEDCT_US_2023_03_01:734990008 UMLS_CUI:C3150878 |
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