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DO Term : sickle cell anemia [DOID:10923] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A sickle cell disease that is characterized by the replacement of both of the beta-globin subunits in hemoglobin with hemoglobin S, resulting in a low number of red blood cells, repeated infections, and periodic episodes of pain.
  • synonyms:
  • NCI:C34676,
  • UMLS_CUI:C0002895,
  • DOID:12924,
  • Hb-S/Hb-C disease,
  • UMLS_CUI:C0019034,
  • Sickle-cell/Hb-C disease without crisis,
  • sickle cell anaemia,
  • ICD9CM:282.63,
  • DOID:13024,
  • Hb SC disease,
  • Hemoglobin S disease without crisis,
  • drepanocytosis,
  • MESH:D006450,
  • NCI:C34383,
  • GARD:8614,
  • ICD10CM:D57.2,
  • Hb-SS disease without crisis,
  • homozygous sickle cell disease,
  • MESH:D000755,
  • SNOMEDCT_US_2023_03_01:35434009,
  • SNOMEDCT_US_2023_03_01:154798006,
  • hemoglobin SC disease,
  • HbSS disease,
  • ICD10CM:D57.1,
  • ICD9CM:282.6,
  • haemoglobin SC disease,
  • ORDO:232
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