The association between TMEM67 (Transmembrane Protein 67) and Meckel Syndrome, Type 1 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 variants940
Symptoms133
Compounds0
Trials0
Publications63
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.