CLRN2:Ensemblv90

clarin 2
ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Amber CLRN2 in Mendeliome


Version 1.3802

1 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 1.304

1 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 1.84

2 reviews 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 2.0

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

Amber CLRN2 in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 2.0

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