About   Help   FAQ
Disease Ontology Browser
sickle cell anemia (DOID:10923)
Alliance: disease page
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.13
The Jackson Laboratory