The association between PEX13 (Peroxisomal Biogenesis Factor 13) and Peroxisome Biogenesis Disorder 1b is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources3
Clinical variants5
Symptoms55
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.