Template:Mitochondrial diseases: Difference between revisions

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en>وضاح
m abbr correction
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  | group2 = Primarily [[nervous system]]
  | group2 = Primarily [[nervous system]]
  | list2 =
  | list2 =
* [[Leigh disease]]
* [[Leigh syndrome|Leigh disease]]
* [[Leber's hereditary optic neuropathy|LHON]]
* [[Leber's hereditary optic neuropathy|LHON]]
* [[Neuropathy, ataxia, and retinitis pigmentosa|NARP]]
* [[Neuropathy, ataxia, and retinitis pigmentosa|NARP]]
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** [[MELAS syndrome|MELAS]]
** [[MELAS syndrome|MELAS]]
** [[MERRF syndrome|MERRF]]
** [[MERRF syndrome|MERRF]]
* [[Chronic progressive external ophthalmoplegia|PEO]]
* [[Chronic progressive external ophthalmoplegia|CPEO]]


  | group4 = No primary system
  | group4 = No primary system
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  | group5 = Chromosomal
  | group5 = Chromosomal
  | list5 =
  | list5 =
* ''[[Optic atrophy 1|OPA1]]''
* ''[[Dynamin-like 120 kDa protein|OPA1]]''
** [[Kjer's optic neuropathy]]
** [[Kjer's optic neuropathy]]
* ''[[SARS2]]''
* ''[[SARS2]]''
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[[Category:Genetic disease and disorder templates by mechanism]]
[[Category:Genetic disease and disorder templates by mechanism]]
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Revision as of 23:24, 26 August 2024