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 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CONGENITAL INSENSITIVITY TO PAIN WITH ANHIDROSIS 256800
R-numbers: R78
Signed-off version 1.36
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hereditary Neuropathies, Insensitivity to pain, congenital, with anhidrosis
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Insensitivity to pain, congenital, with anhidrosis, 256800