The association between TPK1 (Thiamin Pyrophosphokinase 1) and Childhood Encephalopathy Due To Thiamine Pyrophosphokinase Deficiency is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic and likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants221
Symptoms2
Compounds0
Trials0
Publications15
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.