NTRK3

neurotrophic receptor tyrosine kinase 3
OMIM: 191316, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red NTRK3 in Familial Hirschsprung Disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.11

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hirschsprung disease
Tags
  • monogenic-polygenic
Red NTRK3 in Monogenic hearing loss


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert