Search Ontology:
Human Disease

sickle cell anemia

Term ID
DOID:10923
Synonyms
  • drepanocytosis
  • haemoglobin SC disease
  • Hb SC disease
  • Hb-S/Hb-C disease
  • Hb-SS disease without crisis
  • HbSS disease
  • Hemoglobin S disease without crisis
  • hemoglobin SC disease
  • homozygous sickle cell disease
  • sickle cell anaemia
  • Sickle-cell/Hb-C disease without crisis
Definition
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. (3)
References
  • GARD:8614
  • ICD10CM:D57.1
  • ICD10CM:D57.2
  • ICD9CM:282.6
  • ICD9CM:282.63
  • MESH:D000755
  • MESH:D006450
  • NCI:C34383
  • NCI:C34676
  • ORDO:232
  • SNOMEDCT_US_2023_03_01:154798006
  • SNOMEDCT_US_2023_03_01:35434009
  • UMLS_CUI:C0002895
  • UMLS_CUI:C0019034
Ontology
Human Disease   ( DOID:10923 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models