The association between ABCA12 (ATP Binding Cassette Subfamily A Member 12) and Congenital Nonbullous Ichthyosiform Erythroderma is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording a causative germline mutation.
Sources2
Clinical variants5
Symptoms14
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.