GUK1

guanylate kinase 1
OMIM: 139270
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 9.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mitochondrial DNA depletion syndrome 21, OMIM:621071, mitochondrial dna depletion syndrome 21, MONDO:0976132
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 10.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mitochondrial DNA depletion syndrome 21, OMIM:621071, mitochondrial dna depletion syndrome 21, MONDO:0976132