DLD

dihydrolipoamide dehydrogenase
OMIM: 238331
PanelMode of inheritanceDetails
7 panels
R-numbers: R57
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dihydrolipoamide dehydrogenase deficiency, 246900
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
DIHYDROLIPOAMIDE DEHYDROGENASE (E3) DEFICIENCY 248600, LEIGH SYNDROME 256000
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dihydrolipoamide dehydrogenase deficiency, 246900, DIHYDROLIPOAMIDE DEHYDROGENASE (E3) DEFICIENCY
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
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dihydrolipoyl dehydrogenase deficiency (Disorders of pyruvate metabolism), Leigh syndrome, Dihydrolipoamide dehydrogenase deficiency, 246900
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 6.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dihydrolipoamide dehydrogenase deficiency, 246900, Leigh syndrome
R-numbers: R63
Signed-off version 3.105
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY, 246900
R-numbers: R316
Signed-off version 1.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY, 246900