Preferred Name |
Hemoglobinopathy |
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Synonyms |
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Definitions |
An inherited disorder of the structure and/or synthesis of hemoglobin, with a variable phenotype expression ranging from benign to severe. |
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ID |
http://purl.obolibrary.org/obo/SCDO_0000552 |
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curator note |
Suggest update to description in NCIT |
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database cross reference |
NCIT:C3092 |
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definition |
An inherited disorder of the structure and/or synthesis of hemoglobin, with a variable phenotype expression ranging from benign to severe. |
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definition source | ||
existence in other ontologies |
Suggest update to description |
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prefixIRI |
SCDO:0000552 |
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prefLabel |
Hemoglobinopathy |
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rdfs:label |
Hemoglobinopathy |
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subClassOf |
Create mapping