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Emery-dreifuss Syndrome
Emery-Dreifuss Syndrome
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Muscular dystrophy
(20)
Becker's muscular dystrophy
Duchenne muscular dystrophy
Dystrophin
Facioscapulohumeral muscular dystrophy
Fukuyama type muscular dystrophy
Fukuyama type muscular dystrophy
Laminopathy
MD CARE Act
Biostrophin
Congenital muscular dystrophy
Darius Goes West
Help Cure Muscular Dystrophy
Jerry Lewis MDA Telethon
Moonrise (Penny Wolfson book)
Muscular dystrophy organizations
Myostatin
Myotonic dystrophy
Oculopharyngeal muscular dystrophy
People with muscular dystrophy
Robert Ross (CEO)
Walker-Warburg syndrome
more...
Genetic disorders
(34)
Charcot-marie-tooth disease type 2b1
Bethlem myopathy
Carnitine Palmityl Transferase Deficiency
Multiple sulfatase deficiency
Zaspopathy
Zaspopathy
Endocardial fibroelastosis
5p- syndrome
Clawhand
Acrocephal- opolysyndactyly
Central core disease
4p- syndrome
Myotonia congenita
Barraquer-Simons Syndrome
Werner syndrome
FPLD
Monosomy
Hutchinson Gilford Progeria Syndrome
Nemaline myopathy
Dejerine-Sottas disease
Dyskeratosis congenita
Paramyotonia congenita
Trisomy
Ellis-van creveld syndrome
McCune Albright syndrome
Adrenoleuk- odystrophy
Acid maltase deficiency
Alport syndrome
Mucopolysa- ccharidosis
Becker's muscular dystrophy
Fukuyama type muscular dystrophy
Muscular dystrophy
Duchenne muscular dystrophy
Laminopathy
Facioscapulohumeral muscular dystrophy
more...
Genodermatoses
(10)
Mandibuloacral dysplasia
Distal Arthrogryposis, Type IIA
Ectodermal dysplasia
Epidermolysis bullosa simplex
Multiple sulfatase deficiency
Multiple sulfatase deficiency
Acrocephal- opolysyndactyly
4p- syndrome
Werner syndrome
Hutchinson Gilford Progeria Syndrome
Dyskeratosis congenita
more...
Conditions of the subcutaneous fat
Familial partial lipodystrophy
Lipodystrophy
Barraquer-Simons Syndrome
Neurology
Limb girdle muscular dystrophy
Muscle weakness
Dystonia
Myasthenia gravis
Aniridia
Muscular dystrophy
Adrenoleuk- odystrophy
Muscular dystrophy organizations
Muscular Dystrophy Association
Myotonic Dystrophy Foundation
Muscular Dystrophy Campaign
Muscular Dystrophy Canada
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
Congenital disorders
Marinesco sjogren syndrome
Macrocephaly
Bethlem myopathy
Endocardial fibroelastosis
Genetics
LMNA
X linked
X-linked recessive
Mutations
Aniridia
Muscular disorders
(23)
Mitochondrial myopathies
Myopathy
Myotubular myopathy
Arthrogryposis
Central core disease
Central core disease
Chronic progressive external ophthalmoplegia
Congenital myopathy
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Muscular dystrophy
Myokmia
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
Diseases and disorders
(58)
Neuromuscular junction disease
Emery-dreifuss muscular dystrophy x-linked
Metatropic dwarfism
Early constraint defects
Morvan disease
Morvan disease
Diencephalic syndrome
Acanthoche- ilonemiasis
Agenesis of corpus callosum
Distal muscular dystrophy
Inflammatory myopathy
Meniscus tear
X-linked mental retardation
Anemia, hemolytic
Cardiomyopathy, dilated
Macular degeneration, age-related
Granulomatosis
Endometrial cancer
Aplasia
Myopathy
Mandibuloacral dysplasia
Becker's muscular dystrophy
Fukuyama type muscular dystrophy
Muscular dystrophy
Duchenne muscular dystrophy
Charcot-marie-tooth disease type 2b1
Limb girdle muscular dystrophy
Distal Arthrogryposis, Type IIA
Bethlem myopathy
Carnitine Palmityl Transferase Deficiency
Marinesco sjogren syndrome
Multiple sulfatase deficiency
Lipodystrophy
Zaspopathy
Endocardial fibroelastosis
5p- syndrome
Clawhand
Acrocephal- opolysyndactyly
Central core disease
Myotubular myopathy
Cardiomyopathy
Werner syndrome
Ectodermal dysplasia
Facioscapulohumeral muscular dystrophy
Hutchinson Gilford Progeria Syndrome
Nemaline myopathy
Lambert eaton syndrome
Epidermolysis bullosa simplex
Dyskeratosis congenita
Mitochondrial myopathies
Paramyotonia congenita
Dystonia
Ellis-van creveld syndrome
Myasthenia gravis
Acid maltase deficiency
Alport syndrome
Macrocephaly
Mucopolysa- ccharidosis
Aniridia
more...
See also
(20)
Diseases and disorders
Autosomal dominant
Autosomal recessive
Myoneural junction
Emerin
Emerin
Lamins
alopecia cicatrisata
Dreifuss
Dysplasia
Mullerian duct
Dentin dysplasia
LMNB1
POMGNT1
Acanthocytosis
Nuclear lamina
Cardiomyopathy
Noncompaction cardiomyopathy
People
Politicians
MYO-029
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