The association between ABCC8 (ATP Binding Cassette Subfamily C Member 8) and Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources2
Clinical variants1
Symptoms28
Compounds0
Trials0
Publications7
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.