Sickle Cell Disease Ontology Project

Variant Sickle Cell Syndrome

http://scdontology.h3abionet.org/ontology/SCDO_0001051

Any hemoglobinopathy in which the sickle mutation is inherited in combination with another globin gene mutation (eg, alpha globin, beta globin, gamma globin). These hemoglobinopathies may have different clinical severity compared with homozygous sickle mutation (HbSS).

Term info

curator note

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definition source

http://www.uptodate.com/contents/overview-of-variant-sickle-cell-syndromes

existence in other ontologies

None

Sickle Cell Disease Variant, SCD Variant, Variant Sickle Cell Syndromes

Term relations

Subclass of:

Sickle Cell Disease