Sickle Cell Disease Ontology Project

Hemoglobin H

http://scdontology.h3abionet.org/ontology/SCDO_0000515

An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in alpha-thalassemia.

Term info

database cross reference

MESH:D006447

database cross reference

MESH:D006447

definition source

http://purl.bioontology.org/ontology/MESH/D006447

existence in other ontologies

Sufficient

Hb H, HbH Hemoglobin, HbH

Term relations

Subclass of:

Abnormal Hemoglobin