SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Hereditary hemoglobinopathy due to globin chain mutation  127038008

Hereditary hemoglobin S  416417002

Sickling disorder due to hemoglobin S  417357006

Double heterozygous sickling disorder   23269001

SNOMED CT code


SNOMED code23269001
nameDouble heterozygous sickling disorder
statusactive
date introduced2002-01-31
fully specified name(s)Double heterozygous sickling disorder (disorder)
synonymsDouble heterozygous sickling disorder
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsSickling disorder due to hemoglobin S   417357006
children
  • Sickle cell-beta-thalassemia   127041004
  • Sickle cell-hemoglobin C disease   35434009
  • Sickle cell-hemoglobin D disease   25472008
  • Sickle cell-hemoglobin E disease   47024008
  • Sickle cell-hemoglobin Lepore disease   127047000
  • Sickle cell-Hemoglobin O Arab disease   127048005
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
            Hereditary hemoglobin S   416417002
              Sickling disorder due to hemoglobin S   417357006
                Double heterozygous sickling disorder   23269001

ancestors
sorted most to least specific
cpt crosswalks

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