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Muscular disorders
(22)
Central core disease
Congenital myopathy
Inclusion body myositis
Mitochondrial myopathy
Muscular dystrophies
Muscular dystrophies
Myotubular myopathy
Nemaline myopathy
Polymyositis
Thyrotoxic Myopathy
X-linked myotubular myopathy
Arthrogryposis
Chronic progressive external ophthalmoplegia
Diastasis recti
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Myokmia
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Torticollis
Writer's cramp
Zenker's degeneration
more...
Medical condition
(50)
Mitochondrial diseases
Distal myopathy
Inflammatory myopathy
Myopathy myotubular
Bethlem myopathy
Bethlem myopathy
Lipid storage myopathy
Idiopathic inflammatory myopathy
Mitochondrial myopathy-e- ncephalopathy-lactic acidosis
Myopathy desmin storage
Proximal myotonic myopathy
Rhabdomyolysis
Neurofibromatosis 2
Neurotic depression
Myopathy with lactic acidosis and sideroblastic anemia
Myxoma
Limb girdle muscular dystrophy
Mucocutaneous lymph node disease
Meralgia paresthetica
Minimal change disease
Myotonia atrophica
Mucopolysa- ccharidosis iii
Munchausens syndrome
Muscle fasciculation
Facial neuropathy
Myxomatous mitral valve
Mucopolysa- ccharidosis iv
Neurogenic arthropathy
Malignant hyperthermia
Necrotizing ulcerative gingivitis
Ophthalmoplegia
Mitral valve stenosis
Mucopolysa- ccharidosis, type I
Periodic paralysis
Mucolipidoses
Acid maltase deficiency
Infectious mononucleosis
Nevoid basal cell carcinoma syndrome
Hypotonia
Mastoiditis
Myelofibrosis
Meningococcal meningitis
Congenital fiber type disproportion
Nemaline myopathy
Myotubular myopathy
Mitochondrial myopathy
Congenital myopathy
X-linked myotubular myopathy
Muscular dystrophies
Central core disease
Polymyositis
more...
Autosomal recessive disorders
Niemann-Pick disease type C
Nemaline myopathy
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Mucolipidoses
Acid maltase deficiency
Genetic disorders
(20)
Myotonia congenita
Myoclonic Epilepsy with Ragged Red Fibers
Multiple lentigines syndrome
Mitochondrial disorders
Nemaline myopathy
Nemaline myopathy
Mitochondrial diseases
Congenital myopathy
Bethlem myopathy
Proximal myotonic myopathy
Neurofibromatosis 2
Muscular dystrophies
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Central core disease
Mucopolysa- ccharidosis, type I
Periodic paralysis
Mucolipidoses
Acid maltase deficiency
Nevoid basal cell carcinoma syndrome
Niemann-Pick disease type C
more...
Neurological disorders
Neuromyotonia
Nemaline myopathy
Myotonia congenita
Meralgia paresthetica
Central core disease
Mitochondrial diseases
(16)
Kearns-Sayre syndrome
Diabetes mellitus and deafness
Friedreich's ataxia
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease
Mitochondrial disorders
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
Mitochondrial myopathy
Myoclonic Epilepsy with Ragged Red Fibers
Myoneurogenic gastrointestinal encephalopathy
Neuropathy, ataxia, and retinitis pigmentosa
Nonsyndromic deafness
Pearson syndrome
Progressive external ophthalmoplegia
Threshold expression
Wolfram syndrome
more...
Neurology
(9)
Critical illness myopathy
Muscle weakness
Proximal myotonic myopathy
Neurofibromatosis 2
Muscular dystrophies
Muscular dystrophies
Limb girdle muscular dystrophy
Ophthalmoplegia
Niemann-Pick disease type C
Mitochondrial disorders
more...
Cardiology
Mitral valve replacement
Myocardial contusion
LDL-C
Myxoma
Mucocutaneous lymph node disease
Muscular system
Muscle biopsy
Muscle Disease
Muscle fasciculation
Muscle weakness
Lysosomal storage diseases
(40)
Acid maltase deficiency
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycoproteinosis
Hunter syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Mucolipidoses
Mucolipidosis type IV
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease type C
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Fibrates
(12)
Fibrate
Gemfibrozil
Lofibra
Aluminium clofibrate
Bezafibrate
Bezafibrate
Ciprofibrate
Clinofibrate
Clofibrate
Clofibride
Etofibrate
Ronifibrate
Simfibrate
more...
Diseases and disorders
(11)
Hereditary inclusion body myopathy
Nabothian cyst
Myotonia
Neuromuscular junction disease
Distal myopathy
Distal myopathy
Bethlem myopathy
Idiopathic inflammatory myopathy
Muscular dystrophies
Mucopolysa- ccharidosis iv
Niemann-Pick disease type C
Meningococcal meningitis
more...
Symptoms
(10)
Muscle function loss
Uncoordinated movement
Nasal flaring
Nail abnormalities
Movement dysfunctional
Movement dysfunctional
Motormental retardation
Facial weakness
Muscle fasciculation
Muscle weakness
Hypotonia
more...
See also
(20)
EPSM
Necrotizing vasculitis
Myofibrillar
HMG CoA
Mevalonate
Mevalonate
Needle cricothyrotomy
Nevus araneus
Altoprev
Statins
Monorchism
Triglide
Nephritis, interstitial
Inclusion body
Statin
Nevus sebaceous
Rosuvastatin
Natal teeth
Common peroneal nerve
Nightmare disorder
Necrotizing pneumonia
more...
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