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Bethlem Myopathy
Bethlem myopathy
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Congenital disorders
Buschke-Ollendorff syndrome
Achondrogenesis type 2
Fibrochondrogenesis
Achondrogenesis type 1B
Diseases and disorders
(14)
Schmid metaphyseal chondrodysplasia
Neuromuscular junction disease
Pelger-Huet anomaly
Zaspopathy
Epidermolysis bullosa dystrophica
Epidermolysis bullosa dystrophica
Osteopoikilosis
Raine syndrome
Chondrodysplasia punctata, rhizomelic
Short rib-polydactyly syndrome
Epidermolysis bullosa simplex
Osteodysplasia
Collagen disease
Congenital muscular dystrophy
Osteochondropathy
more...
Genetic disorders
(31)
Laminopathy
Barraquer-Simons Syndrome
Marshall syndrome
Collagenopathy, types II and XI
Hypochondrogenesis
Hypochondrogenesis
Becker's muscular dystrophy
Thomsen disease
Otospondyl- omegaepiphyseal dysplasia
Paramyotonia congenita
Multiple epiphyseal dysplasia
Merrf
Nemaline myopathy
Boomerang dysplasia
Central core disease
Spondyloepiphyseal dysplasia congenita
Zunich Kaye syndrome
Atelosteogenesis, type II
Congenital myopathy
Eem syndrome
Gerodermia osteodysplastica
Familial cutaneous papillomatosis
Lelis syndrome
Alport syndrome
Stickler syndrome
Dejerine Sottas syndrome
Buschke-Ollendorff syndrome
Pelger-Huet anomaly
Zaspopathy
Fibrochondrogenesis
Raine syndrome
Congenital muscular dystrophy
more...
Medical condition
(39)
Ichthyosis bullosa of siemens
Scleroatonic muscular dystrophy
Centronuclear myopathy
Inflammatory myopathy
Steatocystoma multiplex
Steatocystoma multiplex
Hyperkalemic
Camurati engelmann disease
Lambert-eaton myasthenic syndrome
Ollier disease
Bullous pemphigoid
Chondromatous
Limb girdle muscular dystrophy
Myopathy
Hypokalemic
Achondrogenesis type 2
Marshall syndrome
Pelger-Huet anomaly
Hypochondrogenesis
Epidermolysis bullosa dystrophica
Becker's muscular dystrophy
Paramyotonia congenita
Multiple epiphyseal dysplasia
Osteopoikilosis
Nemaline myopathy
Boomerang dysplasia
Central core disease
Spondyloepiphyseal dysplasia congenita
Fibrochondrogenesis
Raine syndrome
Zunich Kaye syndrome
Chondrodysplasia punctata, rhizomelic
Short rib-polydactyly syndrome
Congenital myopathy
Eem syndrome
Gerodermia osteodysplastica
Osteodysplasia
Alport syndrome
Stickler syndrome
Congenital muscular dystrophy
more...
Syndromes
(10)
Buschke-Ollendorff syndrome
Laminopathy
Barraquer-Simons Syndrome
Marshall syndrome
Raine syndrome
Raine syndrome
Zunich Kaye syndrome
Eem syndrome
Lelis syndrome
Alport syndrome
Stickler syndrome
more...
Genetic disorder
Buschke-Ollendorff syndrome
Thomsen disease
Merrf
Congenital myopathy
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 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
(20)
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
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...
Structural proteins
Scleroprotein
Anchoring fibrils
Reticular fiber
Gene
(14)
EMID2
COL6A1
COL6A3
COL6A2
COL25A1
COL25A1
COL19A1
COL12A1
COL11A1
COL14A1
COL16A1
COL5A3
COL13A1
COL15A1
COL8A1
more...
See also
(20)
Keratinopathy
Sack-Barabas syndrome
Myoneural junction
Epidermal junctions
Myotonic Dystrophy Foundation
Myotonic Dystrophy Foundation
Procollagen peptidase
MYO-029
Ethanedial
Pentanedial
Neuromyotonia
Emerin
Epidermolytic hyperkeratosis
G.N. Ramachandran
Julian Voss-Andreae
Wandering cell
COL2A1 gene
Nevus flammeus nuchae
Col27a1
The Proteolysis Map
Hospitals
more...
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