OBO ID: DOID:10923
Term Name: sickle cell anemia Search Ontology:
Synonyms:
  • drepanocytosis
  • haemoglobin SC disease
  • Hb SC disease
  • Hb-S/Hb-C disease
  • Hb-SS disease without crisis
  • Hemoglobin S disease without crisis
  • hemoglobin SC disease
  • sickle cell anaemia
  • Sickle-cell/Hb-C disease without crisis
Definition: A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape. (3)
References:
  • GARD:8614
  • ICD10CM:D57.1
  • ICD10CM:D57.2
  • ICD9CM:282.6
  • ICD9CM:282.63
  • MESH:D000755
  • MESH:D006450
  • NCI:C34383
  • NCI:C34676
  • OMIM:603903
  • ORDO:232
  • SNOMEDCT_US_2022_03_01:154798006
  • SNOMEDCT_US_2022_03_01:35434009
  • UMLS_CUI:C0002895
  • UMLS_CUI:C0019034
Ontology: Human Disease   (DOID:10923)
OTHER sickle cell anemia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HBB Sickle cell anemia 603903
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None