Pages that link to "Myotonia congenita"
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Showing 50 items.
- Genetic disorder (links | edit)
- Kocher–Debre–Semelaigne syndrome (links | edit)
- Lambert–Eaton myasthenic syndrome (links | edit)
- Muscular dystrophy (links | edit)
- Myasthenia gravis (links | edit)
- Neuromyotonia (links | edit)
- Cystic fibrosis (links | edit)
- List of neurological conditions and disorders (links | edit)
- Febrile seizure (links | edit)
- Brugada syndrome (links | edit)
- Glycogen storage disease (links | edit)
- Staffordshire Bull Terrier (links | edit)
- Long QT syndrome (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Myotonia (links | edit)
- Osteopetrosis (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Congenital insensitivity to pain (links | edit)
- Atrophy (links | edit)
- Malignant hyperthermia (links | edit)
- Erythromelalgia (links | edit)
- Duchenne muscular dystrophy (links | edit)
- Hypotonia (links | edit)
- Hallermann–Streiff syndrome (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Becker muscular dystrophy (links | edit)
- New Forest pony (links | edit)
- Oculopharyngeal muscular dystrophy (links | edit)
- Timothy syndrome (links | edit)
- Fukuyama congenital muscular dystrophy (links | edit)
- Chloride channel (links | edit)
- Jervell and Lange-Nielsen syndrome (links | edit)
- Myopathy (links | edit)
- Romano–Ward syndrome (links | edit)
- Andersen–Tawil syndrome (links | edit)
- Hypoplastic left heart syndrome (links | edit)
- Fainting goat (links | edit)
- Nemaline myopathy (links | edit)
- Channelopathy (links | edit)
- Facioscapulohumeral muscular dystrophy (links | edit)
- Mitochondrial myopathy (links | edit)
- Kearns–Sayre syndrome (links | edit)
- Thomsen disease (redirect page) (links | edit)
- Genetic disorder (links | edit)
- Lambert–Eaton myasthenic syndrome (links | edit)
- Muscular dystrophy (links | edit)
- Myasthenia gravis (links | edit)
- Neuromyotonia (links | edit)
- Cystic fibrosis (links | edit)
- List of neurological conditions and disorders (links | edit)
- Febrile seizure (links | edit)
- Brugada syndrome (links | edit)
- Glycogen storage disease (links | edit)
- Long QT syndrome (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Osteopetrosis (links | edit)
- List of eponymous diseases (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Congenital insensitivity to pain (links | edit)
- Malignant hyperthermia (links | edit)
- Erythromelalgia (links | edit)
- Duchenne muscular dystrophy (links | edit)
- Hypotonia (links | edit)
- Hallermann–Streiff syndrome (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Becker muscular dystrophy (links | edit)
- Oculopharyngeal muscular dystrophy (links | edit)
- Timothy syndrome (links | edit)
- Fukuyama congenital muscular dystrophy (links | edit)
- Chloride channel (links | edit)
- Jervell and Lange-Nielsen syndrome (links | edit)
- Myopathy (links | edit)
- Romano–Ward syndrome (links | edit)
- Andersen–Tawil syndrome (links | edit)
- Hypoplastic left heart syndrome (links | edit)
- Nemaline myopathy (links | edit)
- Channelopathy (links | edit)
- Facioscapulohumeral muscular dystrophy (links | edit)
- Myotonia congenita (links | edit)
- Mitochondrial myopathy (links | edit)
- Kearns–Sayre syndrome (links | edit)
- Hypertonia (links | edit)
- Walker–Warburg syndrome (links | edit)
- Hypokalemic periodic paralysis (links | edit)
- Paramyotonia congenita (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- MELAS syndrome (links | edit)
- Liddle's syndrome (links | edit)
- Zaspopathy (links | edit)
- Bartter syndrome (links | edit)
- Neuromuscular disease (links | edit)
- Ion transporter (links | edit)
- Vitelliform macular dystrophy (links | edit)
- Centronuclear myopathy (links | edit)
- Congenital absence of the vas deferens (links | edit)
- Pseudohypoaldosteronism (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- MERRF syndrome (links | edit)
- Mucolipidosis type IV (links | edit)
- Distal myopathy (links | edit)
- Generalized epilepsy with febrile seizures plus (links | edit)
- Benign familial neonatal seizures (links | edit)
- Catecholaminergic polymorphic ventricular tachycardia (links | edit)
- Spinocerebellar ataxia type 6 (links | edit)
- Episodic ataxia (links | edit)
- Spinocerebellar ataxia type-13 (links | edit)
- Congenital stationary night blindness (links | edit)
- Myotonic dystrophy (links | edit)
- Familial atrial fibrillation (links | edit)
- Congenital myopathy (links | edit)
- Bethlem myopathy (links | edit)
- Dent's disease (links | edit)
- Potassium-aggravated myotonia (links | edit)
- Mecasermin rinfabate (links | edit)
- Chronic progressive external ophthalmoplegia (links | edit)
- Paroxysmal extreme pain disorder (links | edit)
- CLCN1 (links | edit)
- Thyrotoxic myopathy (links | edit)
- Oculodentodigital dysplasia (links | edit)
- Central core disease (links | edit)
- Ocular albinism (links | edit)
- Neuromuscular junction disease (links | edit)
- Metabolic myopathy (links | edit)
- Ichthyosis hystrix (links | edit)
- Erythrokeratodermia variabilis (links | edit)
- Keratitis–ichthyosis–deafness syndrome (links | edit)
- Clouston's hidrotic ectodermal dysplasia (links | edit)
- Progressive symmetric erythrokeratodermia (links | edit)
- Transient neonatal diabetes (links | edit)
- EAST syndrome (links | edit)
- Ullrich congenital muscular dystrophy (links | edit)
- X-linked myotubular myopathy (links | edit)
- Bart–Pumphrey syndrome (links | edit)
- Thyrotoxic periodic paralysis (links | edit)
- Myopathy, X-linked, with excessive autophagy (links | edit)
- Jules Sottas (links | edit)
- Emily's Entourage (links | edit)
- List of ICD-9 codes 320–389: diseases of the nervous system and sense organs (links | edit)
- Temple–Baraitser syndrome (links | edit)
- Transient neonatal myasthenia gravis (links | edit)
- Talk:Thomsen disease (links | edit)
- User:Katiekillick/sandbox (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User:Evaldez03/sandbox (links | edit)
- User:Pdesai93/sandbox (links | edit)
- User:Nwbeeson/sandbox/Glutamate Gated Chloride Channel (links | edit)
- User:Y-S.Ko/Wikipedia course/Diseases (links | edit)
- User:Yaqi Zhao/sandbox/Channelopathy/skeleton muscle (links | edit)
- User talk:X!/Archives/6/2010 (links | edit)
- User talk:X!/Archives/7/2010 (links | edit)
- User talk:X!/Archives/9/2010 (links | edit)
- User talk:X!/Archives/11/2010 (links | edit)
- User talk:X!/Archives/12/2010 (links | edit)
- User talk:X!/Archives/2/2011 (links | edit)
- User talk:Ebe123/News (links | edit)
- User talk:Crohnie/Archive 6 (links | edit)
- User talk:The Master of Mayhem/Archive 6 (links | edit)
- User talk:X!/Archives/8/2011 (links | edit)
- User talk:X!/Archives/10/2011 (links | edit)
- User talk:X!/Archives/1/2012 (links | edit)
- User talk:Onceonthisisland/Archive 4 (links | edit)
- Wikipedia:WikiProject Medicine/Neurology task force/List of articles (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/NA-, ???-importance medicine articles (links | edit)
- Wikipedia:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Template:Diseases of myoneural junction and muscle (links | edit)
- Template:Channelopathy (links | edit)
- Hypertonia (links | edit)
- Walker–Warburg syndrome (links | edit)
- Hypokalemic periodic paralysis (links | edit)
- Paramyotonia congenita (links | edit)
- Chromosome 7 (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- MELAS syndrome (links | edit)