OTOA

otoancorin
OMIM: 607038, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green OTOA in Mendeliome


Version 1.4216

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 22, MIM# 607039
Tags
  • SV/CNV

Green OTOA in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.317

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 22, MIM# 607039
Tags
  • SV/CNV

Green OTOA in Additional findings_Paediatric


Level 2: Screening
Version 0.280

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Deafness, autosomal recessive

Green OTOA in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 1.147

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BabySeq Category A gene
Phenotypes
  • Deafness, autosomal recessive 22, MIM#607039
Tags
  • SV/CNV
  • deafness