1. Genes and Genomic Entities
  2. ERBB2

ERBB2

erb-b2 receptor tyrosine kinase 2
OMIM: 164870, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red ERBB2 in Paediatric pseudo-obstruction syndrome


Version 1.5
Latest signed off version: v1.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
Phenotypes
  • Visceral neuropathy, familial, 2, autosomal recessive, OMIM:619465