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Autosomal dominant hypophosphatemic rickets

^ http://www.orpha.net/ORDO/Orphanet_89937


Autosomal dominant hypophosphatemic rickets (ADHR) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia.

Synonyms: Autosomal dominant hypophosphatemia, ADHR

Term info

database cross reference
  • UMLS:C0342642 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C1704375 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:E83.3 (NTBT (narrower term maps to a broader term))
  • ICD-10:E83.3 (Attributed)
  • OMIM:193100 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

UMLS:C0342642, UMLS:C1704375, OMIM:193100, ICD-10:E83.3

notation

ORPHA:89937