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Distal Muscular Dystrophy
Distal muscular dystrophy
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Diseases and disorders
(56)
Muscular dystrophy
Duchenne muscular dystrophy
Myotonic dystrophy
Myopathy
Limb girdle muscular dystrophy
Limb girdle muscular dystrophy
Oculopharyngeal muscular dystrophy
Congenital muscular dystrophy
Becker's muscular dystrophy
Complex regional pain syndrome
Bethlem myopathy
Facioscapulohumeral muscular dystrophy
Congenital hypomyelination
Spinal muscular atrophy
Camptomelic syndrome
Neuromuscular junction disease
Polymyositis
Charcot-Marie Tooth Disease
Chromosome 9 trisomy
Chromosome 9 tetrasomy 9p
Chromosome 5 trisomy 5p
Zaspopathy
Myotonic dystrophy type 2
Anonychia onychodystrophy
Ophthalmoplegic muscular dystrophy
Congenital myopathy
Spondyloep- imetaphyseal dysplasia, Strudwick type
Hypotonia
Central core disease
Lactate dehydrogenase deficiency
Myotonic
Paget disease of bone
Centronuclear myopathy
Mitochondrial myopathies
5p- syndrome
Lipodystrophy
Diencephalic syndrome
Mandibuloacral dysplasia
Craniofacial dysostosis
Craniosynostosis
Myasthenia gravis
Dermatomyositis
Lambert-eaton myasthenic syndrome
Myoadenylate deaminase deficiency
Frontotemporal dementia
Cutis laxa
Inflammatory myopathy
Dwarfism
Achalasia
Paramyotonia congenita
Motor neuropathy
HMSN
Diffuse esophageal spasm
Friedreich ataxia
Werdnig-Hoffman disease
Spinal and bulbar muscular atrophy
Polyneuropathy
more...
Neurology
Muscle weakness
Neuronopathy
Muscular dystrophy
Myotonic dystrophy
Limb girdle muscular dystrophy
Myasthenia gravis
Frontotemporal dementia
Muscular system
Dystrophin
Neuromuscular disease
Muscle biopsy
Motor unit
Neurological disorders
(12)
Dejerine-Sottas disease
Laminopathy
Complex regional pain syndrome
Charcot-Marie Tooth Disease
Zaspopathy
Zaspopathy
Central core disease
Lambert-eaton myasthenic syndrome
Paramyotonia congenita
HMSN
Friedreich ataxia
Spinal and bulbar muscular atrophy
Polyneuropathy
more...
Muscular dystrophy organizations
Muscular Dystrophy Association
Myotonic Dystrophy Foundation
Muscular Dystrophy Campaign
Muscular Dystrophy Canada
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
Chromosomes
Chromosome 10
Chromosome 4
Chromosome 11
Gene
Merosin
POMGNT1
Myotilin
Dysferlin
Human body
Demyelinating
Gastrocnemius
Vocal fold
Motor neuron
Muscular disorders
(23)
Arthrogryposis
Central core disease
Centronuclear myopathy
Chronic progressive external ophthalmoplegia
Congenital myopathy
Congenital myopathy
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathies
Muscular dystrophy
Myokmia
Myopathy
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
Muscular dystrophy
(21)
MD CARE Act
Becker's muscular dystrophy
Biostrophin
Congenital muscular dystrophy
Darius Goes West
Darius Goes West
Duchenne muscular dystrophy
Dystrophin
Emery-Dreifuss muscular dystrophy
Facioscapulohumeral muscular dystrophy
Fukuyama congenital muscular dystrophy
Help Cure Muscular Dystrophy
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
Muscular dystrophy organizations
Myostatin
Myotonic dystrophy
Oculopharyngeal muscular dystrophy
People with muscular dystrophy
Robert Ross (CEO)
Walker-Warburg syndrome
more...
See also
(20)
Contractures
Autosomal dominant
Autosomal recessive
Myoneural junction
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy
Titin
Distal
Muscular atrophy
X linked
Dysferlin
Dreifuss
Voluntary muscles
Stamulumab
Retrograde ureteral
MDCC
Random plasma renin
Denervation
Barium swallow
FKRP
Spinal atrophy
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