MT-TE

mitochondrially encoded tRNA glutamic acid
OMIM: 590025
PanelMode of inheritanceDetails
2 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 5.6
MITOCHONDRIAL
Phenotypes
MYOPATHY, MITOCHONDRIAL, WITH DIABETES MELLITUS, DIABETES AND DEAFNESS, MATERNALLY INHERITED, MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 6.4
MITOCHONDRIAL
Phenotypes
MYOPATHY, MITOCHONDRIAL, WITH DIABETES MELLITUS, DIABETES AND DEAFNESS, MATERNALLY INHERITED, MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT