loading...| Preferred Name |
sickle cell anemia |
|
| Synonyms |
Hb-S/Hb-C disease |
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| Definitions |
OMIM mapping confirmed by DO. [LS]. 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. |
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| ID |
http://purl.obolibrary.org/obo/DOID_10923 |
|
| comment |
OMIM mapping confirmed by DO. [LS]. |
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| database_cross_reference |
ICD9CM:282.6 ICD9CM:282.63 MESH:D006450 UMLS_CUI:C0019034 SNOMEDCT_US_2023_03_01:154798006 SNOMEDCT_US_2023_03_01:35434009 MESH:D000755 UMLS_CUI:C0002895 OMIM:603903 ICD10CM:D57.2 ICD10CM:D57.1 GARD:8614 NCI:C34383 NCI:C34676 ORDO:232 |
|
| 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. |
|
| 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 |
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| has material basis in | ||
| has_alternative_id |
DOID:12924 DOID:13024 |
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| has_obo_namespace |
disease_ontology |
|
| id |
DOID:10923 |
|
| in_subset | ||
| label |
sickle cell anemia |
|
| notation |
DOID:10923 |
|
| prefLabel |
sickle cell anemia |
|
| subClassOf |