The association between RTEL1 (Regulator Of Telomere Elongation Helicase 1) and Dyskeratosis Congenita, Autosomal Recessive 5 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.
Sources4
Clinical variants3,285
Symptoms25
Compounds0
Trials0
Publications34
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.