SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Hereditary hemoglobinopathy due to globin chain mutation  127038008

Hemoglobin C disease  51053007

Hemoglobin C beta thalassemia   1148910003

SNOMED CT code


SNOMED code1148910003
nameHemoglobin C beta thalassemia
statusactive
date introduced2021-07-31
fully specified name(s)Hemoglobin C beta thalassemia (disorder)
synonyms
  • Hemoglobin C beta thalassemia
  • Haemoglobin C beta thalassaemia
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Hemoglobin C disease   51053007
  • Autosomal recessive hereditary disorder   85995004
children
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Hereditary hemoglobinopathy due to globin chain mutation   127038008
            Hemoglobin C disease   51053007
              Hemoglobin C beta thalassemia   1148910003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Hemoglobin C beta thalassemia   1148910003

ancestors
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cpt crosswalks

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