CLDN2

claudin 2
OMIM: 300520, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CLDN2 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Susceptibility to pancreatitis
  • Azoospermia, obstructive, with nephrolithiasis, MIM# 301060

Red CLDN2 in Pancreatitis


Level 2: Gastroenterological disorders
Version 1.6

review Other
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Susceptibility to pancreatitis