(Q32139634)
English
congenital muscular dystrophy 1B
congenital muscular dystrophy characterized by autosomal recessive inheritance of proximal muscle weakness, muscle hypertrophy, and early respiratory failure that has material basis in variation in the chromosome region 1q42
- CMD1B
- congenital muscular dystrophy type 1B
- MDC1B
- MUSCULAR DYSTROPHY, CONGENITAL, 1B
- MUSCULAR DYSTROPHY, CONGENITAL, 1B; MDC1B
Statements
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Identifiers
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