Kosmix
One sec... we're building your guide for
Congenital Muscular Dystrophy
Congenital muscular dystrophy
Overview
Anatomy
Health Providers & Organizations
Main ›
Anatomy
›
Body Maps
Layers:
(click to view/hide)
+
Zoom
-
Search:
Related in the Kosmos
?
Muscular dystrophy
(20)
Becker muscular dystrophy
Duchenne muscular dystrophy
Dystrophin
Emery-Dreifuss muscular dystrophy
Facioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy
Fukuyama congenital muscular dystrophy
MD CARE Act
Myotonic dystrophy
Oculopharyngeal muscular dystrophy
Walker Warburg syndrome
Biostrophin
Darius Goes West
Help Cure Muscular Dystrophy
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
Muscular dystrophy organizations
Myostatin
People with muscular dystrophy
Robert Ross (CEO)
more...
Genetic disorders
(27)
Nemaline myopathy
Congenital myopathy
Spinal muscular atrophy
Charcot-Marie Tooth Disease
Spinal muscular atrophy type 1
Spinal muscular atrophy type 1
Bethlem myopathy
Acid maltase deficiency
Metachromatic leukodystrophy
Spinocerebellar ataxia
Morquio syndrome
Mucopolysa- ccharidosis
Carnitine deficiency
Partial trisomy
Microphthalmia
Central core disease
Myotonia congenita
Stickler syndrome
Fabry disease
Fukuyama congenital muscular dystrophy
Muscular dystrophies
Becker muscular dystrophy
Myotonic dystrophy
Duchenne muscular dystrophy
Facioscapulohumeral muscular dystrophy
Oculopharyngeal muscular dystrophy
Emery-Dreifuss muscular dystrophy
Walker Warburg syndrome
more...
Diseases and disorders
(49)
Limb girdle muscular dystrophy
Myopathies
Myotonia
Complex regional pain syndrome
Idiopathic scoliosis
Idiopathic scoliosis
Lissencephaly
Distal muscular dystrophy
Hypotonia
Mitochondrial myopathy
X-linked mental retardation
Ophthalmoplegia
Muscle eye brain disease
Malignant hyperthermia
Neuromuscular junction disease
Dystrophinopathy
Glycogen storage disease
Minicore disease
Familial dysautonomia
Polymyosit- is-dermatomyositis
Sarcoglycanopathies
Metatropic dwarfism
Syndactyly
Arthrogryposis
Cone-rod dystrophy
Clubfoot
Lambert-eaton myasthenic syndrome
Fukuyama congenital muscular dystrophy
Muscular dystrophies
Becker muscular dystrophy
Myotonic dystrophy
Duchenne muscular dystrophy
Nemaline myopathy
Congenital myopathy
Facioscapulohumeral muscular dystrophy
Spinal muscular atrophy
Oculopharyngeal muscular dystrophy
Charcot-Marie Tooth Disease
Spinal muscular atrophy type 1
Bethlem myopathy
Acid maltase deficiency
Metachromatic leukodystrophy
Morquio syndrome
Mucopolysa- ccharidosis
Carnitine deficiency
Partial trisomy
Microphthalmia
Central core disease
Stickler syndrome
Fabry disease
more...
Genetic disorder
Fukuyama congenital muscular dystrophy
Congenital myopathy
Oculopharyngeal muscular dystrophy
Walker Warburg syndrome
Neurology
Muscle weakness
Muscular dystrophies
Limb girdle muscular dystrophy
Myotonic dystrophy
Walker Warburg syndrome
Ophthalmoplegia
Muscular system
Muscle biopsy
Neuromuscular disease
Muscular disorders
Dystrophin
Muscular dystrophy organizations
Muscular Dystrophy Association
Muscular Dystrophy Campaign
Muscular Dystrophy Canada
Myotonic Dystrophy Foundation
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
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
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Medicine
Contractures
Kyphoscoliosis
Age of onset
Diseases and disorders
Genetics
Gene
X-linked recessive
X linked
Genetic disorders
Gene
Merosin
Dysferlin
POMGNT1
POMT1
POMT2
Caveolin 3
Myotilin
Proteins
SEPN1
Sarcoglycan
Selenoprotein
Dysferlin
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 myopathy
Muscular dystrophies
Myokmia
Myopathies
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
See also
(20)
Dreifuss
Autosomal recessive
Autosomal dominant
Decreased muscle tone
Congenital
Congenital
Voluntary muscles
Micropolygyria
FKRP
Myoneural junction
Neuronal migration
Americans with Disabilities Act of 1990
Dystroglycan
Lamin A
Charleston brace
MYO-029
Necrotizing vasculitis
Ryanodine receptor
O-Mannosyl- transferase
Calpain
Retinal dysplasia
more...
more categories...
Health Providers & Organizations
›
Vitals.com
