RIPK2

receptor interacting serine/threonine kinase 2
OMIM: 603455, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red RIPK2 in Infantile enterocolitis & monogenic inflammatory bowel disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.43

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list