SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Hereditary metabolic disease  1821000146108

Hereditary hypertyrosinemia  271847005

Tyrosinemia type I   410056006

SNOMED CT code


SNOMED code410056006
nameTyrosinemia type I
statusactive
date introduced2004-07-31
fully specified name(s)Tyrosinemia type I (disorder)
synonyms
  • Tyrosinaemia type I
  • Tyrosinemia type I
attributes - group1
Due toDeficiency of fumarylacetoacetase   124536006
parents
  • Hereditary hypertyrosinemia   271847005
  • Clinical manifestation of enzyme deficiency   410053003
  • Hereditary cancer-predisposing syndrome   699346009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Hereditary metabolic disease   1821000146108
          Hereditary hypertyrosinemia   271847005
            Tyrosinemia type I   410056006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Clinical manifestation of enzyme deficiency   410053003
          Tyrosinemia type I   410056006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary cancer-predisposing syndrome   699346009
            Tyrosinemia type I   410056006

ancestors
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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.

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