SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Hereditary hemoglobinopathy due to globin chain mutation  127038008

Hemoglobin D disease   66729008

SNOMED CT code


SNOMED code66729008
nameHemoglobin D disease
statusactive
date introduced2002-01-31
fully specified name(s)Hemoglobin D disease (disorder)
synonyms
  • Hemoglobin D disease
  • Hemoglobin D-D disease
  • Haemoglobin D disease
  • Haemoglobin D-D disease
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsHereditary hemoglobinopathy due to globin chain mutation   127038008
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 D disease   66729008

ancestors
sorted most to least specific
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