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Severe Paediatric Disorders v0.12 MYO6 Louise Daugherty reviewed gene: MYO6: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 MYO6 Louise Daugherty Publications for gene MYO6 were updated from to 30847515
Severe Paediatric Disorders v0.11 MYO6 Louise Daugherty Mode of inheritance for gene MYO6 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.10 MYO6 Louise Daugherty Added phenotypes Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, 606346; Deafness, autosomal dominant 22, 606346; Deafness, autosomal recessive 37, 607821 for gene: MYO6
Severe Paediatric Disorders v0.9 MYO6 Louise Daugherty Added phenotypes Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, 606346; Deafness, autosomal dominant 22, 606346; Deafness, autosomal recessive 37, 607821 for gene: MYO6
Severe Paediatric Disorders v0.9 MYO6 Louise Daugherty Added phenotypes Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, 606346; Deafness, autosomal dominant 22, 606346; Deafness, autosomal recessive 37, 607821 for gene: MYO6
Severe Paediatric Disorders v0.8 MYO6 Louise Daugherty Added phenotypes Deafness, autosomal recessive 37, 607821; Deafness, autosomal dominant 22, 606346; Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, 606346 for gene: MYO6
Severe Paediatric Disorders v0.7 MYO6 Louise Daugherty Source Next Generation Children Project was added to MYO6.
Severe Paediatric Disorders v0.5 MYO6 Louise Daugherty Source Expert Review Green was added to MYO6.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 MYO6 Louise Daugherty gene: MYO6 was added
gene: MYO6 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: MYO6 was set to