Genomics England
GMS Panels
Panels
Genes and Entities

NTRK1

neurotrophic receptor tyrosine kinase 1
OMIM: 191315
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CONGENITAL INSENSITIVITY TO PAIN WITH ANHIDROSIS 256800
Green
in Hereditary neuropathy or pain disorder
R-numbers: R78
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hereditary Neuropathies, Insensitivity to pain, congenital, with anhidrosis, OMIM:256800
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Insensitivity to pain, congenital, with anhidrosis, 256800