loading...| Preferred Name | sickle cell anemia | |
| Synonyms |
Hb-S/Hb-C disease Hemoglobin S disease without crisis Hb-SS disease without crisis hemoglobin SC disease Hb SC disease haemoglobin SC disease sickle cell anaemia drepanocytosis Sickle-cell/Hb-C disease without crisis |
|
| 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 |
ICD9CM:282.6 ICD9CM:282.63 MESH:D006450 UMLS_CUI:C0019034 SNOMEDCT_US_2020_03_01:154798006 MESH:D000755 UMLS_CUI:C0002895 SNOMEDCT_US_2020_03_01:35434009 OMIM:603903 ICD10CM:D57.2 ICD10CM:D57.1 GARD:8614 NCI:C34383 NCI:C34676 ORDO:232 |
|
| has exact synonym |
Hb-S/Hb-C disease Hemoglobin S disease without crisis Hb-SS disease without crisis hemoglobin SC disease Hb SC disease haemoglobin SC disease sickle cell anaemia drepanocytosis Sickle-cell/Hb-C disease without crisis |
|
| has_alternative_id |
DOID:12924 DOID:13024 |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:10923 |
|
| imported from | ||
| 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. |
|
| subClassOf |