SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Hemochromatosis type 4   719975002

SNOMED CT code


SNOMED code719975002
nameHemochromatosis type 4
statusactive
date introduced2017-01-31
fully specified name(s)Autosomal dominant hereditary hemochromatosis (disorder)
synonyms
  • Hemochromatosis type 4
  • Haemochromatosis type 4
  • Autosomal dominant hereditary hemochromatosis
  • Autosomal dominant hereditary haemochromatosis
  • Ferroportin disease
  • Hemochromatosis due to defect in ferroportin
  • Haemochromatosis due to defect in ferroportin
attributes - group1
Causative agentIron and/or iron compound   767270007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary hemochromatosis   35400008
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 dominant hereditary disorder   11164009
              Hemochromatosis type 4   719975002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Hereditary metabolic disease   1821000146108
          Hereditary hemochromatosis   35400008
            Hemochromatosis type 4   719975002

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.

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