Sickle Cell Disease Ontology Project

Hemoglobin O-Arab Disease

http://scdontology.h3abionet.org/ontology/SCDO_0000544

A very rare autosomal recessive hemoglobinopathy characterized by an abnormal form of hemoglobin called hemoglobin O-Arab. It is associated with a mild to moderate anemia.

Term info

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definition source

http://www.wardelab.com/14-3.html, http://onlinelibrary.wiley.com/doi/10.1002/pbc.24414/pdf

Homozygous Hemoglobin O-Arab, Hb O-Arab Disease, Homozygous Hb O-Arab