ELMOD3

ELMO domain containing 3
OMIM: 615427, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ELMOD3 in Mendeliome


Version 1.2374

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 1.213

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

Red ELMOD3 in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.67

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