TRMT1

tRNA methyltransferase 1
OMIM: 611669
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
autosomal recessive intellectual disorder, ARID, Mental retardation, autosomal recessive 68, 618302, Global developmental delay, Intellectual disability