Sickle Cell Disease Ontology Project

Sickle Cell Disease-S/O-Arab

http://scdontology.h3abionet.org/ontology/SCDO_0001064

One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin O-Arab. It can cause anemia, repeated infections, and periodic episodes of pain and organ damage.

Term info

curator note

Request inclusion into relevant ontology

dc:source

https://www.cancertherapyadvisor.com/labmed/anemia-associated-with-hemoglobin-s-o-arab/article/612377/

definition source

http://newbornscreeningcodes.nlm.nih.gov/nb/sc/condition/Hb-F-S-O-Arab

existence in other ontologies

Few but definitions not freely available

Hb F,S,O-Arab, Hb S O-Arab disease, Hb S,O-Arab, Sickle Cell-Haemoglobin O-Arab Disease, Sickle Cell-Hemoglobin O-Arab Disease, Hemoglobin S O-Arab Disease, SO(Arab) disease