Hemoglobin Genotype EE
The homozygous genotype that involves a substitution of glutamic acid for a lysine at position 26 of beta-globin chains (hemoglobin C mutation) produced by both beta-globin gene (HBB) alleles.
Sickle Cell Disease Ontology Project
Term info
created by
clair ingram
creation date
2018-09-23T14:35:16.327Z
curator note
Request inclusion into relevant ontology
dc:creator
SCDO (Jade Hotchkiss)
Hemoglobin E Genotype, EE Genotype, Haemoglobin Genotype EE, EE Hemoglobin Genotype, beta6Glu>Lys / beta26Glu>Lys