SLC25A36

solute carrier family 25 member 36
OMIM: 616149
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
Hyperinsulinemic hypoglycemia, familial, 8, OMIM:620211
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 10.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hyperinsulinemic hypoglycemia, familial, 8, OMIM:620211