distal myopathy 1 (Q60195033)
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distal muscular dystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the MYH7 gene on chromosome 14q11
- MPD1
- Laing distal myopathy
- Gowers disease
- Distal myopathy type 1
- Laing early-onset distal myopathy
Language | Label | Description | Also known as |
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English | distal myopathy 1 |
distal muscular dystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the MYH7 gene on chromosome 14q11 |
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