Hereditary hemoglobinopathy   427306008

SNOMED CT code


SNOMED code427306008
nameHereditary hemoglobinopathy
statusactive
date introduced2007-07-31
fully specified name(s)Hereditary hemoglobinopathy (disorder)
synonyms
  • Hereditary hemoglobinopathy
  • Hereditary haemoglobinopathy
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
children
  • Hemoglobinopathy Toms River   782880001
  • Hereditary hemoglobinopathy due to globin chain mutation   127038008
  • Hereditary persistence of fetal hemoglobin   191201002
  • Heterozygous hemoglobinopathy   123773003
  • Homozygous hemoglobinopathy   123772008
  • Thalassemia   40108008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Hereditary red blood cell disorder   414394009
            Hereditary hemoglobinopathy   427306008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Hemoglobinopathy   80141007
            Hereditary hemoglobinopathy   427306008

ancestors
sorted most to least specific
cpt crosswalks

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