NRG3

neuregulin 3
OMIM: 605533, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber NRG3 in Familial Hirschsprung Disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.10

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Alder Hey - Erasmus MC
Phenotypes
  • susceptibility to Hirschsprung disease
Tags
  • cnv