Preferred Name | Thalassemia | |
Synonyms |
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|
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. |
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ID |
http://purl.obolibrary.org/obo/NCIT_C35069 |
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ALT_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. |
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code |
C35069 |
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Contributing_Source |
Cellosaurus CPTAC NICHD |
|
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. |
|
in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 http://purl.obolibrary.org/obo/NCIT_C158520 http://purl.obolibrary.org/obo/NCIT_C156952 http://purl.obolibrary.org/obo/NCIT_C158035 http://purl.obolibrary.org/obo/NCIT_C132009 |
|
label |
Thalassemia |
|
Legacy Concept Name |
Thalassemia |
|
Preferred_Name |
Thalassemia |
|
prefixIRI |
NCIT:C35069 |
|
prefLabel |
Thalassemia |
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Semantic_Type |
Disease or Syndrome |
|
UMLS_CUI |
C0039730 |
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subClassOf |