CLRN2

clarin 2
Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber CLRN2 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Non-syndromic hearing loss
  • Deafness, autosomal recessive 117, MIM# 619174

Amber CLRN2 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.194

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Non-syndromic hearing loss
  • Deafness, autosomal recessive 117, MIM# 619174

Amber CLRN2 in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.63

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Non-syndromic hearing loss
  • Deafness, autosomal recessive 117, MIM# 619174