COCH

cochlin
OMIM: 603196, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green COCH in Mendeliome Version 1.3499	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 9, MIM# 601369 Deafness, autosomal recessive 110, MIM# 618094
Green COCH in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.238	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 9, MIM# 601369 Deafness, autosomal recessive 110, MIM# 618094
Green COCH in Deafness_Isolated Level 2: Hearing and ear disorders Version 1.82	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Melbourne Genomics Health Alliance Deafness Flagship Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 9, MIM# 601369 Deafness, autosomal recessive 110, MIM# 618094
Green COCH in Additional findings_Paediatric Level 2: Screening Version 0.278	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene Phenotypes Deafness, autosomal dominant 9, MIM# 601369 Deafness, autosomal recessive 110, MIM# 618094
Green COCH in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene Phenotypes Deafness, autosomal recessive 110, MIM# 618094 Tags deafness