Hemoglobin Genotype O-Arab
The homozygous genotype that involves a substitution of glutamic acid for a lysine at position 121 of beta-globin chains (hemoglobin O-Arab mutation) produced by both beta-globin gene (HBB) alleles.
Sickle Cell Disease Ontology Project
Term info
created by
clair ingram
creation date
2018-09-23T14:37:20.484Z
curator note
Probably not necessary to include in other ontologies.
dc:creator
SCDO (Jade Hotchkiss)
O-Arab Hemoglobin Genotype, beta121Glu>Lys / beta121Glu>Lys, Haemoglobin Genotype O-Arab, O-Arab Genotype