Pages that link to "Mitochondrial neurogastrointestinal encephalopathy syndrome"
The following pages link to Mitochondrial neurogastrointestinal encephalopathy syndrome
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Showing 50 items.
- Lambert–Eaton myasthenic syndrome (links | edit)
- Muscular dystrophy (links | edit)
- Myasthenia gravis (links | edit)
- Neuromyotonia (links | edit)
- Adenosine monophosphate deaminase deficiency type 1 (links | edit)
- Mitochondrial disease (links | edit)
- Glycogen storage disease (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Hyperuricemia (links | edit)
- Leigh syndrome (links | edit)
- Adenosine deaminase deficiency (links | edit)
- Duchenne muscular dystrophy (links | edit)
- Hypotonia (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Becker muscular dystrophy (links | edit)
- Oculopharyngeal muscular dystrophy (links | edit)
- Lesch–Nyhan syndrome (links | edit)
- Inborn errors of metabolism (links | edit)
- Non-Mendelian inheritance (links | edit)
- Fukuyama congenital muscular dystrophy (links | edit)
- Myopathy (links | edit)
- Human genetics (links | edit)
- Friedreich's ataxia (links | edit)
- Leber's hereditary optic neuropathy (links | edit)
- Nemaline myopathy (links | edit)
- Xanthinuria (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)
- MELAS syndrome (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Hypouricemia (links | edit)
- Adenine phosphoribosyltransferase deficiency (links | edit)
- Kjer's optic neuropathy (links | edit)
- Zaspopathy (links | edit)
- Adenylosuccinate lyase deficiency (links | edit)
- Neuromuscular disease (links | edit)
- Centronuclear myopathy (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- MERRF syndrome (links | edit)
- Distal myopathy (links | edit)
- Dihydropyrimidine dehydrogenase deficiency (links | edit)
- Nucleic acid metabolism (links | edit)
- Pyruvate carboxylase deficiency (links | edit)