TMTC2

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Red TMTC2 in Mendeliome Version 1.3098	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 122, MIM# 620714 Tags disputed
Red TMTC2 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.222	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 dominant Deafness, autosomal recessive 122, MIM# 620714
Red TMTC2 in Deafness_Isolated Level 2: Hearing and ear disorders Version 1.74	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 Deafness, autosomal recessive 122, MIM# 620714 Tags disputed

3 panels