Parent term(s)
Term with siblings
congenital merosin-deficient muscular dystrophy 1A
congenital muscular dystrophy 1B
congenital muscular dystrophy due to integrin alpha-7 deficiency
congenital muscular dystrophy due to LMNA mutation
congenital muscular dystrophy with cataracts and intellectual disability
congenital muscular dystrophy with rapid progression
megaconial type congenital muscular dystrophy
muscular dystrophy-dystroglycanopathy +
rigid spine muscular dystrophy 1
Ullrich congenital muscular dystrophy +
Walker-Warburg syndrome
Bethlem myopathy +
congenital merosin-deficient muscular dystrophy 1A
congenital muscular dystrophy 1B
congenital muscular dystrophy due to integrin alpha-7 deficiency
congenital muscular dystrophy due to LMNA mutation
congenital muscular dystrophy with cataracts and intellectual disability
congenital muscular dystrophy with rapid progression
megaconial type congenital muscular dystrophy
muscular dystrophy-dystroglycanopathy +
rigid spine muscular dystrophy 1
Ullrich congenital muscular dystrophy +
Walker-Warburg syndrome
denotes an 'is-a' relationship