ELMOD3

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Amber ELMOD3 in Mendeliome Version 1.1891	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 88, MIM# 615429 Deafness, autosomal dominant 81, MIM# 619500
Amber ELMOD3 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.194	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 88, MIM# 615429 Deafness, autosomal dominant 81, MIM# 619500
Amber ELMOD3 in Deafness_Isolated Level 2: Hearing and ear disorders Version 1.63	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber 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

3 panels