Term Name:	congenital muscular dystrophy merosin-positive
Synonyms:
Definition:	A congenital muscular dystrophy characterized by autosomal recessive inheritance of generalized muscle weakness and hypotonia without arthrogryposis or central nervous system involvement that has_material_basis_in mutation in the chromosome region 4p16.3.
Ontology:	Human Disease [DOID:0110638]   (DOID:0110638)