Preferred Name |
thalassemia |
|
Synonyms |
sickle-cell thalassemia with crisis sickle-cell thalassemia without crisis thalassemia Hb-S disease without crisis thalassemia Hb-S disease with crisis |
|
Definitions |
An inherited blood disorder characterized by a decreased synthesis of one of the polypeptide chains that form hemoglobin. Anemia results from this abnormal hemoglobin formation. |
|
ID |
http://purl.obolibrary.org/obo/MONDO_0000984 |
|
closeMatch |
http://identifiers.org/snomedct/191182000 http://identifiers.org/snomedct/267521001 http://identifiers.org/snomedct/191193003 http://identifiers.org/snomedct/267557006 http://identifiers.org/snomedct/84188003 |
|
database_cross_reference |
DOID:10241 ICD10:D56.9 COHD:30978 ICD9:282.40 ICD10:D56 EFO:1001996 ICD9:282.49 GARD:0007756 MESH:D013789 SCTID:40108008 UMLS:C0039730 ICD9:282.4 NCIT:C35069 |
|
disease has feature | ||
exactMatch |
http://identifiers.org/snomedct/40108008 http://identifiers.org/mesh/D013789 http://purl.obolibrary.org/obo/DOID_10241 |
|
has exact synonym |
sickle-cell thalassemia with crisis sickle-cell thalassemia without crisis thalassemia Hb-S disease without crisis thalassemia Hb-S disease with crisis |
|
id |
MONDO:0000984 |
|
imported from | ||
label |
thalassemia |
|
notation |
MONDO:0000984 |
|
prefLabel |
thalassemia |
|
textual definition |
An inherited blood disorder characterized by a decreased synthesis of one of the polypeptide chains that form hemoglobin. Anemia results from this abnormal hemoglobin formation. |
|
excluded subClassOf | ||
subClassOf |