CLDN9

claudin 9
OMIM: 615799, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green CLDN9 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Deafness, autosomal recessive 116, MIM#619093

Green CLDN9 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.194

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Deafness, autosomal recessive 116, MIM#619093

Green CLDN9 in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.63

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
  • Literature
Phenotypes
  • Deafness, autosomal recessive 116, MIM#619093

Red CLDN9 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.113

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Deafness, autosomal recessive 116 MIM#619093