Category:Mitochondrial diseases

From Wikipedia, the free encyclopedia

The main article for this category is Mitochondrial disease.

Pages in category "Mitochondrial diseases"

The following 18 pages are in this category, out of 18 total. Updates to this list can occasionally be delayed for a few days.

  • Mitochondrial disease

D

  • Diabetes mellitus and deafness

F

  • Friedreich's ataxia

K

  • Kearns-Sayre syndrome

L

  • Leber's hereditary optic neuropathy
  • Leigh's disease

M

  • MERRF syndrome
  • Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
  • Mitochondrial myopathy
  • Myoneurogenic gastrointestinal encephalopathy

N

  • Neuropathy, ataxia, and retinitis pigmentosa
  • Nonsyndromic deafness

P

  • Pearson syndrome

P cont.

  • Progressive external ophthalmoplegia
  • Pyruvate carboxylase deficiency
  • Pyruvate dehydrogenase deficiency

T

  • Threshold expression

W

  • Wolfram syndrome
Categories: Genetic disorders | Mitochondrial genetics
Views
  • Category
  • Discussion
  • Current revision
Navigation
  • Main Page
  • Contents
  • Featured content
  • Current events
Interaction
  • About Wikipedia
  • Community portal
  • Recent changes
  • Contact Wikipedia
  • Donate to Wikipedia
  • Help
Languages
  • Polski
  • Русский
Powered by MediaWiki
Wikimedia Foundation
  • This page was last modified 18:26, 4 June 2008 by Wikipedia user Kaganer. Based on work by Wikipedia user(s) Kauczuk, Biophys and Apers0n.
  • All text is available under the terms of the GNU Free Documentation License. (See Copyrights for details.)
    Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a U.S. registered 501(c)(3) tax-deductible nonprofit charity.
  • About Wikipedia
  • Disclaimers