Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Alpha-B Crystallinopathy with Cataract
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis
Bassoe Syndrome
Becker muscular dystrophy +
congenital disorder of glycosylation It
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism
congenital muscular dystrophy +
Danon disease
distal myopathy +
Duchenne muscular dystrophy +
Emery-Dreifuss muscular dystrophy +
facioscapulohumeral muscular dystrophy +
Glycogen Storage Disease 0, Liver
Glycogen Storage Disease 0, Muscle
glycogen storage disease I +
glycogen storage disease II +
glycogen storage disease III +
glycogen storage disease IV +
glycogen storage disease IX +
glycogen storage disease V
glycogen storage disease VI
glycogen storage disease VII
An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant.
glycogen storage disease VIII
Glycogen Storage Disease XI
Glycogen Storage Disease XII
Glycogen Storage Disease XIII
glycogen storage disease XV
lethal congenital glycogen storage disease of heart
limb-girdle muscular dystrophy +
Muscular Dystrophy, Animal +
Muscular Dystrophy, Barnes Type
Muscular Dystrophy, Cardiac Type
Muscular Dystrophy, Mabry Type
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries
Myofibrillar Myopathy, ZASP-Related
Myopathy with Abnormal Lipid Metabolism
MYOPATHY, SCAPULOHUMEROPERONEAL
myotonic disease +
oculopharyngeal muscular dystrophy +
Oculopharyngodistal Myopathy +
Polyglucosan Body Disease, Adult Form
Polyglucosan Body Myopathy 1 with or without Immunodeficiency