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
congenital muscular dystrophy with rapid progression
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