Sickle Cell Disease Ontology Project

Delta Beta Thalassemia

http://scdontology.h3abionet.org/ontology/SCDO_0000343

A form of beta-thalassemia characterized by decreased or absent synthesis of the delta- and beta-globin chains with a compensatory increase in expression of fetal gamma-chain synthesis.

Term info

database cross reference

ORPHA:231237

database cross reference

ORPHA:231237

definition source

http://www.orpha.net/ORDO/Orphanet_231237

existence in other ontologies

Sufficient

F Thalassaemia, Delta-Beta-Thalassemia, Delta-Beta-Thalassaemia, Delta Beta Thalassaemia

Term relations

Subclass of:

Beta Thalassemia

Related from:

causes condition

HBB and HBD Deletion

causes or contributes to condition

Crossover between delta (HBD) and beta globin (HBB) gene loci