Kosmix
One sec... we're building your guide for
Myotonia Congenita
Myotonia congenita
Overview
Anatomy
Main ›
Anatomy ›
Anatomy
›
Body Maps
Layers:
(click to view/hide)
+
Zoom
-
Search:
Related in the Kosmos
?
Channelopathy
(42)
Hyperkalemic periodic paralysis
Malignant hyperthermia
Mucolipidosis type 4
Paramyotonia congenita
Periodic paralyses
Periodic paralyses
Potassium-- aggravated myotonia
Achromatopsia
Andersen-Tawil syndrome
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant polycystic kidney
Bartter syndrome
Benign familial neonatal convulsions
Brugada syndrome
Calciumopathy
Channelome
Childhood absence epilepsy
Congenital hyperinsulinism
Congenital insensitivity to pain
Cystic fibrosis
Episodic ataxia
Erythromelalgia
Familial atrial fibrillation
Familial hemiplegic migraine
Focal segmental glomerulosclerosis
Generalized epilepsy with febrile seizures plus
Hypokalemic periodic paralysis
Hypokalemic sensory overstimulation
Hypomagnesemia with secondary hypocalcemia
Juvenile myoclonic epilepsy
Long QT syndrome
Maculopathy
Nonsyndromic deafness
Paroxysmal extreme pain disorder
Pseudohypo- aldosteronism
Retinitis pigmentosa
Rolandic epilepsy
Romano-Ward syndrome
Short QT syndrome
Spinocerebellar ataxia type-13
Spinocerebellar ataxia type-6
Timothy syndrome
X-linked congenital stationary night blindness
more...
Musculoskeletal disorders
Thomsen disease
Potassium-- aggravated myotonia
Neurological disorders
(10)
Progressive sclerosing poliodystrophy
Zaspopathy
Central core disease
Bernhardt-Roth syndrome
Myopathies, nemaline
Myopathies, nemaline
Multiple system atrophy
Accessory nerve disorder
Neuromyotonia
Thomsen disease
Paramyotonia congenita
more...
Genetic disorders
(32)
Myoclonic Epilepsy with Ragged Red Fibers
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Multiple lentigines syndrome
Multiple lentigines syndrome
Mucolipidoses
Myotonic dystrophy
Adrenoleuk- odystrophy
Clawhand
Becker's muscular dystrophy
Fukuyama type muscular dystrophy
Muscular dystrophy
Bethlem myopathy
Muscular dystrophy - Duchenne type
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
McArdle syndrome
Congenital myopathy
Multiple sulfatase deficiency
Muenke syndrome
Emery-Dreifuss muscular dystrophy
Genetic disorder
Phosphofructokinase deficiency
Thomsen disease
Paramyotonia congenita
Potassium-- aggravated myotonia
Zaspopathy
Mucolipidosis type 4
Central core disease
Hyperkalemic periodic paralysis
Periodic paralyses
Myopathies, nemaline
Channelopathies
more...
Neurology
(10)
Myoclonic Encephalopathy of infants
Ramsay Hunt syndrome type I
Muscle weakness
Temporal arteritis
Medulloblastoma
Medulloblastoma
Lgmd
Neurological disorders
Myotonic dystrophy
Adrenoleuk- odystrophy
Muscular dystrophy
more...
Cardiology
Mucocutaneous lymph node disease
Myocardial contusion
Myxoma
Myocarditis
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Mucolipidoses
Mucolipidosis type 4
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Muscular system
Muscle fasciculation
Dystrophin
Contractures
Muscle weakness
Muscular dystrophy
(20)
Becker's muscular dystrophy
Biostrophin
Congenital muscular dystrophy
Darius Goes West
Dystrophin
Dystrophin
Emery-Dreifuss muscular dystrophy
Facioscapulohumeral muscular dystrophy
Fukuyama type muscular dystrophy
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
Muscular Dystrophy Community Assistance Research and Education Amendments of 2001
Muscular dystrophy - Duchenne type
Muscular dystrophy organizations
Myostatin
Myotonic dystrophy
Oculopharyngeal muscular dystrophy
People with muscular dystrophy
Robert Ross (CEO)
Walker-Warburg syndrome
more...
Ion channels
CLCN1
Sodium channel
SCN4A
Chloride channel
Channelopathies
Muscular dystrophy organizations
Muscular Dystrophy Association
Myotonic Dystrophy Foundation
Muscular Dystrophy Campaign
Muscular Dystrophy Canada
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
Diseases and disorders
(12)
Myotonic
Neuromuscular junction disease
Megarectum
Mucous retention cyst
Neurological disorders
Neurological disorders
Mucopolysa- ccharidosis iv
Muscular dystrophy
Bethlem myopathy
Zaspopathy
Multiple sulfatase deficiency
Myositis ossificans
Phosphofructokinase deficiency
more...
Symptoms
(9)
Movement dysfunctional
Motormental retardation
Muscle function loss
Uncoordinated movement
Muscle stiffness
Muscle stiffness
Muscle atrophy
Dysphagia
Muscle fasciculation
Muscle weakness
more...
Muscular disorders
(23)
Centronuclear myopathy
Myopathies
Arthrogryposis
Central core disease
Chronic progressive external ophthalmoplegia
Chronic progressive external ophthalmoplegia
Congenital myopathy
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathies
Muscular dystrophy
Myokmia
Myopathies, nemaline
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
Medical condition
(51)
Myotonia atrophica
Myxomatous mitral valve
Infectious mononucleosis
Morvan disease
Metatropic dwarfism
Metatropic dwarfism
Phytanic acid storage disease
Myopathy myotubular
Melnick-needles syndrome
Mesangiocapillary glomerulonephritis
Progressive osseous heteroplasia
Meningococcal
Mucocutaneous lymph node disease
Mucopolysa- ccharidosis iii
Munchausens syndrome
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Muscle fasciculation
Mucolipidoses
Myopathies
Paramyotonia congenita
Myxoma
Myotonic dystrophy
Progressive sclerosing poliodystrophy
Clawhand
Becker's muscular dystrophy
Fukuyama type muscular dystrophy
Muscular dystrophy
Muscle stiffness
Bethlem myopathy
Centronuclear myopathy
Muscular dystrophy - Duchenne type
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
Mucolipidosis type 4
Central core disease
Marinesco sjogren syndrome
Malignant hyperthermia
Hyperkalemic periodic paralysis
Periodic paralyses
Congenital myopathy
Bernhardt-Roth syndrome
Myopathies, nemaline
Mitochondrial myopathies
Multiple system atrophy
Muenke syndrome
Myositis ossificans
Myocarditis
Myelodysplastic syndromes
Temporal arteritis
Medulloblastoma
Lgmd
Phosphofructokinase deficiency
more...
See also
(20)
Munchausens syndrome
Monorchism
Fainting goats
Midface trauma
Myoneural junction
Myoneural junction
Hirayama syndrome
Autosomal dominant
Dominance (genetics)
Marinesco sjogren syndrome
Phosphates
Sodium phosphates
Uro-KP-Neutral
Mycosis fungoides
Aspiration pneumonia
EMG
Genetic counseling
Muscle biopsy
Anemia, macrocytic
Muscle glycogen phosphorylase
Mitochondrial myopathies
more...
more categories...
Health Providers & Organizations
›
Vitals.com
