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


Level 2: Gastrohepatology
Version 2.5
Latest signed off version: v2.0 (30 Apr 2025)

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