tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2
OMIM: 615047
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Intellectual developmental disorder with autistic features and language delay, with or without seizures, 618906