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sickle cell anemia (DOID:10923)
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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
Alt IDs: DOID:12924, DOID:13024, ICD10CM:D57.1, ICD10CM:D57.2, ICD9CM_2006:282.63, ICD9CM:282.6, ICD9CM:282.60, ICD9CM:282.63, MESH:D000755, MESH:D006450, NCI:C34383, NCI:C34676, ORDO:232, UMLS_CUI:C0002895, UMLS_CUI:C0019034
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.

Disease References using Mouse Models (31)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
07/02/2024
MGI 6.13
The Jackson Laboratory