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Oculopharyngeal Muscular Dystrophy
Oculopharyngeal muscular dystrophy
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Genetic disorder
Fukuyama type muscular dystrophy
Thomsen disease
Congenital myopathy
Rare diseases
Leukodystrophy, globoid cell
Zaspopathy
Multiple sulfatase deficiency
Lambert-eaton myasthenic syndrome
Muscular dystrophy
(20)
Becker's muscular dystrophy
Congenital muscular dystrophy
Duchenne muscular dystrophy
Dystrophin
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy
Facioscapulohumeral muscular dystrophy
MD CARE Act
Myostatin
Myotonic muscular dystrophy
Biostrophin
Darius Goes West
Fukuyama type muscular dystrophy
Help Cure Muscular Dystrophy
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
Muscular dystrophy organizations
People with muscular dystrophy
Robert Ross (CEO)
Walker-Warburg syndrome
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Genetic disorders
(24)
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Adrenoleuk- odystrophy
Bethlem myopathy
Galactosemias
Galactosemias
Dejerine-Sottas disease
Spinal muscular atrophy
Charcot-Marie Tooth Disease
Central core disease
Osteogenesis imperfecta
Paramyotonia congenita
Muscular dystrophy
Duchenne muscular dystrophy
Becker's muscular dystrophy
Fukuyama type muscular dystrophy
Facioscapulohumeral muscular dystrophy
Leukodystrophy, globoid cell
Myotonic muscular dystrophy
Emery-Dreifuss muscular dystrophy
Congenital muscular dystrophy
Zaspopathy
Multiple sulfatase deficiency
Thomsen disease
Congenital myopathy
more...
Diseases and disorders
(58)
Limb girdle muscular dystrophy
Myopathies, structural, congenital
Distal muscular dystrophy
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Neuromuscular junction disease
Olfaction disorders
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Postpoliomyelitis syndrome
Polyendocr- inopathies, autoimmune
Encephalitis, arbovirus
Intervertebral disk displacement
Morvan disease
Optic neuropathy, ischemic
Rosenthal syndrome
Complex regional pain syndrome
Metatropic dwarfism
Brachial plexus neuropathies
Mitochondrial myopathies
Polymyositis
Myotonic
Nephroptosis
Myelodysplastic syndromes
Myotubular myopathy
Marinesco sjogren syndrome
Dermatomyositis
Achalasia
Inflammatory myopathy
Diffuse esophageal spasm
Meniscus tear
Myasthenia gravis
Ophthalmoplegia
Muscular dystrophy
Duchenne muscular dystrophy
Becker's muscular dystrophy
Fukuyama type muscular dystrophy
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Facioscapulohumeral muscular dystrophy
Leukodystrophy, globoid cell
Myotonic muscular dystrophy
Congenital muscular dystrophy
Bethlem myopathy
Zaspopathy
Galactosemias
Multiple sulfatase deficiency
Spinal muscular atrophy
Charcot-Marie Tooth Disease
Central core disease
Osteogenesis imperfecta
Paramyotonia congenita
Lambert-eaton myasthenic syndrome
Congenital myopathy
more...
Neurology
Muscle weakness
Muscular dystrophy
Limb girdle muscular dystrophy
Adrenoleuk- odystrophy
Myotonic muscular dystrophy
Myasthenia gravis
Ophthalmoplegia
Muscular dystrophy organizations
Muscular Dystrophy Association
Muscular Dystrophy Campaign
Myotonic Dystrophy Foundation
Muscular Dystrophy Canada
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
Somatic motor system
(13)
Motor unit
Muscle fibers
Myoneural junction
Alpha motor neuron
Bereitscha- ftspotential
Bereitscha- ftspotential
Lower motor neuron
Memory Cells (Motor Cortex)
Motor cortex
Motor unit recruitment
Primary motor cortex
Stretch reflex
Supplementary motor area
Upper motor neuron
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Muscular system
(8)
Neuromuscular disease
Muscle cells
Involuntary muscles
Muscle biopsy
Dystrophin
Dystrophin
Motor unit
Muscular disorders
Muscle fibers
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Muscular disorders
(23)
Inclusion body myositis
Arthrogryposis
Central core disease
Chronic progressive external ophthalmoplegia
Congenital myopathy
Congenital myopathy
Diastasis recti
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathies
Muscular dystrophy
Myokmia
Myopathies, structural, congenital
Myotubular myopathy
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
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See also
(20)
PABPN1
MY0-029
Autosomal dominant
Autosomal recessive
Dreifuss
Dreifuss
Contractures
Oropharyngeal dysphagia
Upper esophageal sphincter
Mullerian duct
Poly A-binding protein
Muscle wasting
X linked
Americans with Disabilities Act of 1990
Muscular disorders
Mouse model
Myotomy
Oculocutaneous albinism
Proximal
Stem cell therapy
Bolus (medicine)
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