The association between HBG1 (Hemoglobin Subunit Gamma 1) and Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome is a manually-curated gene–disease association, with its 2 contributing sources — 1 of them expert-curated — recording a causative germline mutation.
Sources2
Clinical variants1
Symptoms6
Compounds0
Trials0
Publications2
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.