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

Sickle cell-hemoglobin C disease   35434009

SNOMED CT code


SNOMED code35434009
nameSickle cell-hemoglobin C disease
statusactive
date introduced2002-01-31
fully specified name(s)Sickle cell-hemoglobin C disease (disorder)
synonyms
  • Hb SC disease
  • Sickle cell hemoglobin C
  • Sickle cell haemoglobin C
  • Double heterozygous for Hb S and Hb D
  • Sickle cell-haemoglobin C disease
  • Sickle cell anaemia with haemoglobin C disease
  • Haemoglobin S/C disease
  • Hemoglobin S/C disease
  • Sickle cell anemia with hemoglobin C disease
  • Haemoglobin S-C disease
  • Sickle cell-hemoglobin C disease
  • Hemoglobin S-C disease
  • HbS-HbC disease
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Double heterozygous sickling disorder   23269001
  • Mixed hemoglobin disorder   38589006
children
  • Sickle cell-hemoglobin C disease with crisis   417517009
  • Sickle cell-hemoglobin C disease without crisis   417683006
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
                  Sickle cell-hemoglobin C disease   35434009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Hemoglobinopathy   80141007
            Mixed hemoglobin disorder   38589006
              Sickle cell-hemoglobin C disease   35434009

ancestors
sorted most to least specific
cpt crosswalks

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