CLDN9

claudin 9
OMIM: 615799, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CLDN9 in COVID-19 research


Level 2: Viral research
Version 1.141

review Unknown
Sources
  • Expert list
  • OMIM
  • Expert Review Red
Green CLDN9 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.25
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Expert
    Phenotypes
    • Deafness, autosomal recessive 116, OMIM:619093
    • deafness, autosomal recessive 116, MONDO:0033670