Sickle Cell Disease Ontology Project

Sickle Cell Disease-S/HPFH

http://scdontology.h3abionet.org/ontology/SCDO_1000010


A group of disorders caused by large deletions of the beta-globin gene complex; typically 30% fetal haemoglobin.

Term info

curator note

Request inclusion into relevant ontology

definition source

http://ac.els-cdn.com/S014067361061029X/1-s2.0-S014067361061029X-main.pdf?_tid=691c25c0-5826-11e7-b704-00000aacb35e&acdnat=1498230953_4d1264c47385275daf8fc2a1e1de62e3

Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome, Sickle Cell Disease Syndrome-Hereditary Persistence of Fetal Hemoglobin, Sickle Cell Disease-S/Persistence of Fetal Hemoglobin, Sickle Cell-Hereditary Persistence of Fetal Hemoglobin, HPFH-Sickle Cell Disease Syndrome