SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Hereditary metabolic disease  1821000146108

Hereditary xanthinuria  54627004

Hereditary xanthinuria type 1   836343001

SNOMED CT code


SNOMED code836343001
nameHereditary xanthinuria type 1
statusactive
date introduced2020-07-31
fully specified name(s)Hereditary xanthinuria type 1 (disorder)
synonyms
  • Hereditary xanthinuria type 1
  • Xanthinuria type I
attributes - group2
Finding siteKidney structure   64033007
parentsHereditary xanthinuria   54627004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Hereditary metabolic disease   1821000146108
          Hereditary xanthinuria   54627004
            Hereditary xanthinuria type 1   836343001

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

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