Sickle Cell Disease Ontology Project

Heterozygous Deletion of HBA1 or HBA2

http://scdontology.h3abionet.org/ontology/SCDO_1000239

Deletion of one alpha-globin gene, either an HBA1 or HBA2 gene, which results in Alpha Thalassemia Silent (the person with the mutation is a silent carrier).

Term info

curator note

Request inclusion into relevant ontology

dc:creator

SCDO (Jade Hotchkiss)

existence in other ontologies

None

Term relations

Subclass of:

Alpha-Globin Locus Deletion

Related from:

has contributing genetic variation

Alpha Thalassemia Silent Genotype