C0272080_NCI_NICHD | Knowledge4COVID-19

Property	Value
?:definition	An autosomal recessive disorder resulting from the production of hemoglobin D, secondary to various substitution mutations in the beta chain, and characterized by mild hemolytic anemia and possible splenomegaly. Multiple subtypes of hemoglobin D have been identified.
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?:hasGeneratedBy	<https://research.tib.eu/covid-19/SourceName/NCI_NICHD>
?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

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