loading...| Preferred Name |
Thalassemia |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35069 |
| 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. |
| code |
C35069 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C158520 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156952 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C158035 |
| Contributing_Source |
CPTAC NICHD Cellosaurus |
| 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. |
| FULL_SYN |
Thalassemia |
| label |
Thalassemia |
| Legacy Concept Name |
Thalassemia |
| Preferred_Name |
Thalassemia |
| prefixIRI |
Thesaurus:C35069 |
| prefLabel |
Thalassemia |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0039730 |
| subClassOf |