NAV3

neuron navigator 3
OMIM: 611629, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber NAV3 in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • recessive neurodevelopmental disorder
    Tags
    • Q1_25_ promote_green