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DO Term : adenine phosphoribosyltransferase deficiency [DOID:0060350] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A purine-pyrimidine metaobolic disorder characterized by the formation 2,8-dihydroxyadenine stones and renal failure secondary to intratubular crystalline precipitation and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding adenine phosphoribosyltransferase (APRT) on chromosome 16q24.
  • synonyms:
  • UMLS_CUI:C3665382,
  • APRT deficiency,
  • 2,8-dihydroxyadenine urolithiasis,
  • GARD:10666,
  • 614723,
  • SNOMEDCT_US_2023_03_01:11852004,
  • MESH:C538228,
  • OMIM:614723,
  • NCI:C121564,
  • GARD:546,
  • UMLS_CUI:C0268120
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