Sickle Cell Disease Ontology Project

Hemoglobin Genotype CC

http://scdontology.h3abionet.org/ontology/SCDO_1000232

The homozygous genotype that involves a substitution of glutamic acid for a lysine at position 6 of beta-globin chains (hemoglobin C mutation) produced by both beta-globin gene (HBB) alleles.

Term info

created by

clair ingram

creation date

2018-09-23T14:38:06.452Z

curator note

Request inclusion into relevant ontology

dc:creator

SCDO (Jade Hotchkiss)

beta6Glu>Lys / beta6Glu>Lys, Haemoglobin Genotype CC, CC Genotype, Hemoglobin C Genotype, CC Hemoglobin Genotype

Term relations

Subclass of: