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loading...| Preferred Name |
Hemoglobin H disease |
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| Synonyms |
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| Definitions |
(HBH): A form of alpha- thalassemia due to the loss of three alpha genes. This results in high levels of a tetramer of four beta chains (hemoglobin H), causing a severe and life-threatening anemia. Untreated, most patients die in childhood or early adolescence. |
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| ID |
http://purl.obolibrary.org/obo/OMIM_613978 |
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| definition |
(HBH): A form of alpha- thalassemia due to the loss of three alpha genes. This results in high levels of a tetramer of four beta chains (hemoglobin H), causing a severe and life-threatening anemia. Untreated, most patients die in childhood or early adolescence. |
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cell_cycle_ontology |
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| id |
OMIM:613978 |
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| label |
Hemoglobin H disease |
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| notation |
OMIM:613978 |
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| prefLabel |
Hemoglobin H disease |
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