NAV3

neuron navigator 3
OMIM: 611629
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
Signed-off version 11.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
recessive neurodevelopmental disorder