Sickle Cell Disease Ontology Project

Hemoglobin Trait

http://scdontology.h3abionet.org/ontology/SCDO_0000550

A condition in which a person is heterozygous for a globin gene, with one normal allele and one defective allele.

Term info

curator note

NCIT includes this class below "Hemoglobinopathy", hence its inclusion here.

definition source

http://bioportal.bioontology.org/ontologies/NCIT/?p=classes&conceptid=http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C95534

Heterozygous Hemoglobinopathy

Term relations

Subclass of: