Preferred Name |
thalassemia |
|
Synonyms |
sickle-cell thalassemia with crisis thalassemia Hb-S disease without crisis sickle-cell thalassemia 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 |
|
disease has feature | ||
exactMatch |
http://identifiers.org/snomedct/40108008 http://identifiers.org/mesh/D013789 http://purl.obolibrary.org/obo/DOID_10241 http://purl.bioontology.org/ontology/ICD10CM/D56 |
|
hasDbXref |
NCIT:C35069 ICD9:282.40 ICD9:282.49 ICD10CM:D56 EFO:1001996 UMLS:C0039730 SCTID:40108008 MESH:D013789 DOID:10241 ICD9:282.4 |
|
hasExactSynonym |
sickle-cell thalassemia with crisis thalassemia Hb-S disease without crisis sickle-cell thalassemia without crisis thalassemia Hb-S disease with crisis |
|
IAO_0000115 |
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 |
MONDO:0000984 |
|
inSubset | ||
label |
thalassemia |
|
notation |
MONDO:0000984 |
|
prefLabel |
thalassemia |
|
excluded_subClassOf | ||
subClassOf |