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loading...| Preferred Name |
Compound Heterozygous Sickle Cell Disease |
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| Synonyms |
Compound Heterozygous Sickling Disorder |
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| Definitions |
A hemoglobinopathy in which the sickle mutation (HBB, Glu6Val) is inherited in combination with another beta-globin gene mutation, other thanHBB, Glu6Val. |
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| ID |
http://purl.obolibrary.org/obo/SCDO_1000163 |
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| curator note |
Request inclusion into relevant ontology |
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| dc:creator |
SCDO (Jade Hotchkiss) |
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| definition |
A hemoglobinopathy in which the sickle mutation (HBB, Glu6Val) is inherited in combination with another beta-globin gene mutation, other thanHBB, Glu6Val. |
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| existence in other ontologies |
None |
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| hasExactSynonym |
Compound Heterozygous Sickling Disorder |
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| prefixIRI |
SCDO:1000163 |
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| prefLabel |
Compound Heterozygous Sickle Cell Disease |
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| rdfs:label |
Compound Heterozygous Sickle Cell Disease |
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| subClassOf |