Anemia, Sickle Cell
Disease ID: disease_node_1204
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| Dbxref | 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 |
|---|---|
| Subclassof | DOID_2355, DOID_0050737, DOID_0081445 |
| Data Source | DOID, MESH |
| Synonyms | Hb SC disease, Hb-S/Hb-C disease, Hb-SS disease without crisis, HbSS disease, Hemoglobin S disease without crisis, Sickle-cell/Hb-C disease without crisis, drepanocytosis, haemoglobin SC disease, hemoglobin SC disease, homozygous sickle cell disease, sickle cell anaemia |
| Mesh Id | D000755 |
| Mesh Label | Anemia, Sickle Cell |
| Mesh Subclassof | D000745, D006453 |
| Doid Label | sickle cell anemia |
| Doid Description | 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. OMIM mapping confirmed by DO. [LS]. |
| Has Material Basis In | GENO_0000148, CL_0000232 |
| Disease Node Id | disease_node_1204 |
| Doid Id | DOID_10923 |
| Label | Anemia, Sickle Cell |
| Doid Alternate Ids | DOID_12924, DOID_13024 |
- Outgoing r'ship
SUBCLASS_OFto/from Sickle Cell Disease(ID:disease_node_15319) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Anemia(ID:disease_node_1179) (Disease)
- Incoming r'ship
ASSOCIATED_WITH_DISEASEto/from Adansonia digitata (Plant) Rel Props:Icd11:3A51.1; Doid:DOID_10923; Mesh:D000755; Part:bark; Reference:ISBN:9780387706375; ISBN:9788172362089