Sickle Cell Disease Ontology Project

Compound Heterozygous Sickle Cell Disease

http://scdontology.h3abionet.org/ontology/SCDO_1000163

Any hemoglobinopathy in which the sickle mutation is inherited in the heterozygous state in combination with another globin gene mutation (eg, alpha globin, beta globin, gamma globin) on a different allele, with the affect being the sickling of red blood cells.

Term info

created by

Jade Hotchkiss

creation date

2018-09-04T19:31:56.051Z

curator note

Request inclusion into relevant ontology

dc:creator

SCDO (Jade Hotchkiss)

existence in other ontologies

None

Compound Heterozygous Sickling Disorder, Doubly Heterozygous Sickle Cell Disease, Double Heterozygous Sickle Cell Disease

Term relations

Subclass of:

Variant Sickle Cell Syndrome