Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia
Carey-Fineman-Ziter syndrome +
Chanarin-Dorfman syndrome +
chronic fatigue syndrome
compartment syndrome +
Congenital Myopathy with Neuropathy and Deafness
Congenital Universal Muscular Hypoplasia of Krabbe
Contracture +
Craniomandibular Disorders +
diaphragm disease +
Dimauro Disease
disseminated eosinophilic collagen disease
Ehlers-Danlos syndrome kyphoscoliotic type 2
eosinophilia-myalgia syndrome
A hypereosinophilic syndrome that is characterized by subacute onset of myalgias and peripheral eosinophilia, followed by chronic neuropathy and skin induration. (DO)
Erythrocyte Amp Deaminase Deficiency
Erythrocyte Lactate Transporter Defect
familial periodic paralysis +
fibromyalgia +
Fingerprint Body Myopathy
Gamstorp-Wohlfart syndrome
Granulovacuolar Lobular Myopathy with Electrical Myotonia
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis
Hypertrophia Musculorum Vera
Internal Anal Sphincter Myopathy
Kocher-Debre-Semelaigne Syndrome
Late-Onset Carnitine Palmitoyltransferase II Deficiency
Marinesco-Sjogren syndrome
Medial Tibial Stress Syndrome
Mitochondrial DNA Depletion Syndrome, Myopathic Form +
Muscle Cramp +
Muscle Rigidity +
Muscle Spasticity +
muscle tissue disease +
Muscle Weakness +
Musculoskeletal Pain +
Myalgia +
myeloproliferative disorder with eosinophilia
myofascial pain syndrome +
Myopathic Carnitine Deficiency
Myopathy with Lactic Acidosis, Hereditary
myotonic disease +
Myotoxicity
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
Pdgfra-Associated Chronic Eosinophilic Leukemia
Pectoralis Muscle, Absence of
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss
Proximal Myopathy with Focal Depletion of Mitochondria
pulmonary eosinophilia +
Rhabdomyolysis +
Singleton Merten Syndrome +
Skeletal Muscle Injuries
Skeletal Muscle Reperfusion Injury
systemic primary carnitine deficiency disease
Tel Hashomer Camptodactyly Syndrome
tendinitis +
Treft Sanborn Carey Syndrome
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy