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Term ID: | 10956 |
Name: | Thalassemia |
Definition: | A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. |
Alternative IDs: | |
ParentIDs: | MESH:D000745|MESH:D006453 |
TreeNumbers: | C15.378.071.141.150.875 |C15.378.420.826 |C16.320.070.875 |C16.320.365.826 |
Synonyms: | Thalassemias |
Slim Mappings: | Blood disease|Genetic disease (inborn) |
Reference: |
MedGen: D013789
MeSH: D013789
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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