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Congenital myopathy v3.30 CHCHD10 Arina Puzriakova Phenotypes for gene: CHCHD10 were changed from ?Myopathy, isolated mitochondrial, autosomal dominant 616209; Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 615911; Spinal muscular atrophy, Jokela type 615048 to Myopathy, isolated mitochondrial, autosomal dominant, OMIM:616209; Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, OMIM:615911; Spinal muscular atrophy, Jokela type, OMIM:615048
Congenital myopathy v2.5 CHCHD10 Zornitza Stark Deleted their review
Congenital myopathy v2.5 CHCHD10 Zornitza Stark reviewed gene: CHCHD10: Rating: AMBER; Mode of pathogenicity: None; Publications: 22818856, 25193783; Phenotypes: Congenital myopathy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Congenital myopathy CHCHD10 Anna Sarkozy reviewed CHCHD10
Congenital myopathy CHCHD10 Helen Brittain marked CHCHD10 as ready
Congenital myopathy CHCHD10 Helen Brittain classified CHCHD10 as red
Congenital myopathy CHCHD10 Helen Brittain reviewed CHCHD10