Parent term(s)
congenital muscular dystrophy
+
Term with siblings
muscular dystrophy-dystroglycanopathy +
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
megaconial type congenital muscular dystrophy
rigid spine muscular dystrophy 1
Ullrich congenital muscular dystrophy
+
Walker-Warburg syndrome
Child term(s)
congenital muscular dystrophy-dystroglycanopathy type A
+
muscular dystrophy-dystroglycanopathy type B
+
muscular dystrophy-dystroglycanopathy type C12
muscular dystrophy-dystroglycanopathy type C8
denotes an 'is-a' relationship