autosomal recessive disease sickle cell anemia ICD10CM:D57.2 ICD10CM:D57.1 ICD9CM:282.63 NCI:C34676 UMLS_CUI:C0002895 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. SNOMEDCT_US_2020_03_01:154798006 DOID:13024 MESH:D000755 DOID:12924 DOID:10923 UMLS_CUI:C0019034 ICD9CM:282.6 disease_ontology Hb SC disease OMIM mapping confirmed by DO. [LS]. ORDO:232 NCI:C34383 OMIM:603903 SNOMEDCT_US_2020_03_01:35434009 GARD:8614 MESH:D006450 Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease sickle cell anaemia blood protein disease