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loading...| Preferred Name |
Hemoglobin H Disease |
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| Synonyms |
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| Definitions |
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C95504 |
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| ALT_DEFINITION |
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia. |
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| code |
C95504 |
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| Contributing_Source |
NICHD |
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| definition |
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia. |
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| in_subset | ||
| label |
Hemoglobin H Disease |
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| Preferred_Name |
Hemoglobin H Disease |
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| prefixIRI |
NCIT:C95504 |
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| prefLabel |
Hemoglobin H Disease |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C3161174 |
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| subClassOf |
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