CRYM

crystallin mu
OMIM: 123740, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CRYM in ClinGen Gene Validity Curations


Version 0.65

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • ClinGen
  • Expert Review Red
Phenotypes
  • autosomal dominant nonsyndromic deafness 40
Green CRYM in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.41
Latest signed off version: v4.39 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • NHS GMS
    • Expert
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • UKGTN
    Phenotypes
    • Deafness, autosomal dominant 40, OMIM:616357
    • autosomal dominant nonsyndromic deafness 40, MONDO:0014603