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Muscular Diseases

More information in Books or onNLM PubMed
Definition: Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.  GEN; prefer specifics; inflamm dis   
Examples Arthrogryposis; Compartment Syndromes; Contracture; Craniomandibular Disorders; Eosinophilia-Myalgia Syndrome; Fatigue Syndrome, Chronic; Fibromyalgia; Isaacs Syndrome; Medial Tibial Stress Syndrome; Mitochondrial Myopathies; Muscle Cramp; Muscle Neoplasms; Muscle Rigidity; Muscle Spasticity; Muscle Weakness; Muscular Disorders, Atrophic; Myofascial Pain Syndromes; Myopathies, Structural, Congenital; Myositis; Myotonic Disorders; Paralyses, Familial Periodic; Polymyalgia Rheumatica; Rhabdomyolysis; Tendinopathy 		Other names Myopathy; Myopathic Condition; Muscular Disease; Myopathic Conditions; Muscle Disorder; Myopathies; Muscle Disorders
 
SubstanceCAS Registry & nameCategoriesSource
Mesoectodermal dysplasia  0   *Ellis-Van Creveld Syndrome *Muscular Diseases.
Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia  0   *Bone Diseases, Developmental *Fibrous Dysplasia of Bone *Hand Deformities, Congenital *Muscular Diseases.
Singleton Merten syndrome  0   *Aortic Diseases *Dental Enamel Hypoplasia *Muscular Diseases *Osteoporosis *Odontodysplasia *Vascular Calcification Metacarpus/abnormalities.
Kocher-Debre-Semelaigne syndrome  0   *Congenital Hypothyroidism *Hypertrophy *Muscular Diseases Muscle, Skeletal/pathology.
Tel Hashomer camptodactyly syndrome  0   *Hand Deformities, Congenital *Heart Septal Defects, Atrial *Hirsutism *Muscular Diseases Dermatoglyphics.
Systemic carnitine deficiency  0   *Muscular Diseases *Cardiomyopathies *Hyperammonemia Carnitine/deficiency.
Triglyceride storage disease with impaired long-chain fatty acid oxidation  0   *Lipid Metabolism, Inborn Errors *Muscular Diseases *Ichthyosiform Erythroderma, Congenital.
Treft Sanborn Carey syndrome  0   *Ataxia *Blepharoptosis *Hearing Loss, Sensorineural *Muscular Diseases *Ophthalmoplegia *Optic Atrophy.
Vacuolar myopathy  0   *Muscular Diseases *Lysosomal Storage Diseases.
VLCAD deficiency  0   *Lipid Metabolism, Inborn Errors *Muscular Diseases *Mitochondrial Diseases Acyl-CoA Dehydrogenase, Long-Chain/deficiency.
Dimauro disease  0   *Kidney Diseases *Muscular Diseases Phosphoglycerate Mutase/deficiency.
Myostatin-related muscle hypertrophy  0   *Hypertrophy *Muscular Diseases.
Myopathy, congenital nonprogressive with Moebius and Robin sequences  0   *Muscular Diseases *Pierre Robin Syndrome *Mobius Syndrome.
Myopathic carnitine deficiency  0   *Muscular Diseases Carnitine/deficiency.
Marinesco-Sjogren-like syndrome (MSLS)  0   *Cataract/congenital *Cerebellar Ataxia *Intellectual Disability *Muscular Diseases.
Rippling muscle disease, 1  0   *Muscular Diseases.
Rippling muscle disease  0   *Muscular Diseases.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012
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