SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Hereditary metabolic disease  1821000146108

Hereditary hypertyrosinemia   271847005

SNOMED CT code


SNOMED code271847005
nameHereditary hypertyrosinemia
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary hypertyrosinemia (disorder)
synonyms
  • Tyrosinaemia-tyrosiluria hereditary syndrome
  • Hereditary hypertyrosinemia
  • Hereditary hypertyrosinaemia
  • Tyrosinemia-tyrosiluria hereditary syndrome
  • Hereditary tyrosinaemia
  • Hereditary tyrosinemia
parents
children
  • Fumarylacetoacetase deficiency, chronic type   52452006
  • Hypertyrosinemia, Richner-Hanhart type   4887000
  • Tyrosinemia type I   237916000  removed: 2004-07-31
  • Tyrosinemia type I   410056006
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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of acid-base balance   26436007
          Acidemia   70731005
            Aminoacidemia   46556004
              Hypertyrosinemia   56595005
                Hereditary hypertyrosinemia   271847005

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.