MT-TL1

mitochondrially encoded tRNA leucine 1 (UUA/G)
OMIM: 590050
PanelMode of inheritanceDetails
3 panels
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 5.0
MITOCHONDRIAL
Phenotypes
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 6.0
MITOCHONDRIAL
Phenotypes
R-numbers: R141
Signed-off version 2.2
MITOCHONDRIAL
Phenotypes
MIDD, DIABETES AND DEAFNESS, MATERNALLY INHERITED, Diabetes-Deafness Syndrome, Maternally Transmitted, MELAS syndrome, Maternally inherited diabetes