obsolete_congenital muscular dystrophy without intellectual disability true Orphanet:370980 CMD without intellectual disability Replaced by Mondo term MONDO_1040033 which has the same label. Use: http://purl.obolibrary.org/obo/MONDO_1040033 congenital muscular dystrophy-dystroglycanopathy without intellectual disability 3.88.0 A rare, genetic, congenital muscular dystrophy due to dystroglycanopathy characterized by a wide phenotypic spectrum which includes hypotonia and muscular weakness present at birth or early infancy, delayed or arrested motor development, and normal intellectual abilities with normal (or only mild abnormalities) neuroimaging studies. Feeding difficulties, joint and spinal deformities, and respiratory insufficiency may be associated. Decreased alpha-dystroglycan on immunohistochemical muscle staining and elevated serum creatine kinase are observed. CMD-no MR http://purl.obolibrary.org/obo/MONDO_1040033 Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also.