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Fukuyama Type Muscular Dystrophy
Fukuyama type muscular dystrophy
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Muscular dystrophy
(19)
Congenital muscular dystrophy
Duchenne muscular dystrophy
Dystrophin
Facioscapulohumeral muscular dystrophy
Myotonic dystrophy
Myotonic dystrophy
Walker Warburg syndrome
Becker's muscular dystrophy
Biostrophin
Darius Goes West
Emery-Dreifuss muscular dystrophy
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
Muscular Dystrophy Community Assistance Research and Education Amendments of 2001
Muscular dystrophy organizations
Myostatin
Oculopharyngeal muscular dystrophy
People with muscular dystrophy
Robert Ross (CEO)
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Genetic disorder
Fukuhara Syndrome
Fucosidosis
Walker Warburg syndrome
Genetic disorders
(13)
Multiple sulfatase deficiency
Partial monosomy
Craniofacial dysostosis
Carnitine deficiency
Microphthalmia
Microphthalmia
Muscular dystrophy
Congenital muscular dystrophy
Fukuhara Syndrome
Walker Warburg syndrome
Facioscapulohumeral muscular dystrophy
Fucosidosis
Duchenne muscular dystrophy
Myotonic dystrophy
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Medical condition
(37)
Congenital hypomyelination
Chromosome 9 trisomy
Chromosome 5 trisomy 5p
Camptomelic syndrome
Chromosome 9 tetrasomy 9p
Chromosome 9 tetrasomy 9p
Fiber type disproportion congenital
Fetal aids infection
Muscle eye brain disease
Morvan disease
Metatropic dwarfism
Gouty nephropathy familial
Fiedler Disease
Marinesco sjogren syndrome
Fryns syndrome
Fg syndrome
Myopathy
Cutis laxa
Myotubular myopathy
Limb girdle muscular dystrophy
Complex regional pain syndrome
Mental retardation
Lissencephaly
Craniosynostosis
Myelodysplastic syndromes
Malignant hyperthermia
Meniscus tear
Clubfoot
Muscular dystrophy
Congenital muscular dystrophy
Partial monosomy
Craniofacial dysostosis
Facioscapulohumeral muscular dystrophy
Fucosidosis
Carnitine deficiency
Microphthalmia
Duchenne muscular dystrophy
Myotonic dystrophy
more...
Congenital disorders
Camptodactyly
Macrocephaly
Marinesco sjogren syndrome
Lissencephaly
Clubfoot
Chromosomes
Chromosome 18
Chromosome 10
Chromosome 3
Chromosome 4
Chromosome 11
See also
(20)
Diseases and disorders
Micropolygyria
Merosin
Yoshiki Fukuyama
POMGNT1
POMGNT1
Dystroglycan
Mullerian duct
POMT1
Dysplasia
O-Mannosyl- transferase
FKRP
Febris
Autosomal recessive
Brainstem
Muscle weakness
Fanconi
Femoral triangle
Autosomal dominant
Aplasia
Neil J. Gunther
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