Sickle cell-hemoglobin D disease   25472008

SNOMED CT code


SNOMED code25472008
nameSickle cell-hemoglobin D disease
statusactive
date introduced2002-01-31
fully specified name(s)Sickle cell-hemoglobin D disease (disorder)
synonyms
  • Sickle cell haemoglobin D
  • Sickle cell hemoglobin D
  • Sickle cell-hemoglobin D disease
  • Hemoglobin S-D disease
  • HbS-HbD disease
  • Sickle cell-haemoglobin D disease
  • Double heterozygous for Hb S + Hb D Punjab
  • Haemoglobin S-D disease
  • Hemoglobin S/D Punjab disease
  • Sickle cell anemia with hemoglobin D disease
  • Haemoglobin S/D Punjab disease
  • Sickle cell anaemia with haemoglobin D disease
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Double heterozygous sickling disorder   23269001
  • Mixed hemoglobin disorder   38589006
children
  • Sickle cell-hemoglobin D disease with crisis   417748003
  • Sickle cell-hemoglobin D disease without crisis   416214006
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 D disease   25472008

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 D disease   25472008

ancestors
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