PanelApp
  1. Genes and Genomic Entities
  2. ELMOD3

ELMOD3

ELMO domain containing 3
OMIM: 615427, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red ELMOD3 in Mendeliome


Version 1.3795

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 88, MIM# 615429
  • Deafness, autosomal dominant 81, MIM# 619500

Red ELMOD3 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.304

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 88, MIM# 615429
  • Deafness, autosomal dominant 81, MIM# 619500