NRG3

neuregulin 3
OMIM: 605533, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red NRG3 in Gastrointestinal neuromuscular disease


Level 2: Gastroenterological disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Hirschsprung disease