loading...| Preferred Name |
sickle cell anemia |
| Synonyms |
hemoglobin SC disease |
| Definitions |
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. OMIM mapping confirmed by DO. [LS]. |
| ID |
http://purl.obolibrary.org/obo/DOID_10923 |
| comment |
OMIM mapping confirmed by DO. [LS]. |
| database_cross_reference |
NCI:C34383 ICD10CM:D57.1 ICD9CM:282.6 ICD10CM:D57.2 UMLS_CUI:C0019034 ICD9CM:282.63 NCI:C34676 ORDO:232 SNOMEDCT_US_2020_03_01:35434009 MESH:D006450 UMLS_CUI:C0002895 MESH:D000755 OMIM:603903 GARD:8614 SNOMEDCT_US_2020_03_01:154798006 |
| has exact synonym |
hemoglobin SC disease drepanocytosis Hb SC disease Hb-S/Hb-C disease haemoglobin SC disease Hemoglobin S disease without crisis sickle cell anaemia Sickle-cell/Hb-C disease without crisis Hb-SS disease without crisis |
| has_alternative_id |
DOID:12924 DOID:13024 |
| id |
DOID:10923 |
| in_subset | |
| label |
sickle cell anemia |
| notation |
DOID:10923 |
| prefLabel |
sickle cell anemia |
| textual 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. |
| 引自 | |
| 有_obo_命名空间 |
disease_ontology |
| subClassOf |