SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal recessive hereditary disorder  85995004

Isolated xanthine oxidase deficiency   72682008

SNOMED CT code


SNOMED code72682008
nameIsolated xanthine oxidase deficiency
statusremoved
date introduced2002-01-31
fully specified name(s)Isolated xanthine oxidase deficiency (disorder)
synonyms
  • Isolated xanthine oxidase deficiency
  • Hereditary xanthinuria, type I
parentsAutosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Isolated xanthine oxidase deficiency   72682008  removed: 2023-04-30

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.