Misplaced Pages

The following pages link to Central core disease

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Showing 50 items.

• 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)
• Syncoilin (links | edit)
• Chronic progressive external ophthalmoplegia (links | edit)
• Paroxysmal extreme pain disorder (links | edit)
• Thyrotoxic myopathy (links | edit)
• Oculodentodigital dysplasia (links | edit)
• Ryanodine receptor 1 (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)
• Central core myopathy (redirect page) (links | edit)
  • Congenital myopathy (links | edit)
  • List of neuromuscular disorders (links | edit)
  • User:Joelmills/Table continued (links | edit)
  • User:Brainist/MeSH articles (links | edit)
• Multi/minicore myopathy (links | edit)
• Bart–Pumphrey syndrome (links | edit)
• Thyrotoxic periodic paralysis (links | edit)
• List of OMIM disorder codes (links | edit)
• Myopathy, X-linked, with excessive autophagy (links | edit)
• Central core disease of muscle (redirect page) (links | edit)
  • Talk:Central core disease (links | edit)
• Congenital neuromuscular disease with uniform type 1 fibers (redirect page) (links | edit)
• Emily's Entourage (links | edit)
• List of ICD-9 codes 320–389: diseases of the nervous system and sense organs (links | edit)