myosin light chain 3
OMIM: 160790, Gene2Phenotype
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MYL3 in Hypertrophic cardiomyopathy
Level 3: Cardiomyopathy
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review | BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
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Phenotypes
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MYL3 in Dilated Cardiomyopathy and conduction defects
Level 3: Cardiomyopathy
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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MYL3 in Hereditary neuropathy
Level 3: Motor and Sensory Disorders of the PNS
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review | Not set |
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Phenotypes
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MYL3 in Paediatric or syndromic cardiomyopathy
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review | BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
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Phenotypes
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MYL3 in Hereditary neuropathy or pain disorder
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review | Not set |
Sources
Phenotypes
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