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Category:Mitochondrial diseases

Radiology: Ultrasound · Computed tomography · Magnetic resonance | Anatomical pathology: Histopathology | File format: SVG · Video recording |
<nowiki>malattia mitocondriale; mitokondriális betegség; malaltia mitocondrial; Gaixotasun mitokondrial; mitochondriální onemocnění; أمراض متقدرية; Митохондриальные заболевания; mitokondriyal hastalıklar; Mitochondriopathie; 线粒体疾病; maladie mitochondriale; Միտոքոնդրիումային հիվանդություն; 粒線體疾病; enfermedad mitocondrial; mitohondrijska bolezen; ミトコンドリア病; Mitokondriesykdommer; Mitoxondrial xəstəliklər; Penyakit mitokondria; mitokondriesjukdom; Мітохондріальні хвороби; energiestofwisselingsziekte; 粒線體疾病; Choroby mitochondrialne; mitokondriesjukdom; Mitokondriotaudit; mitochondrial disease; mitokondria malsano; Митохондриски заболувања; نقائص میتوکندریایی; desórdenes resultantes de la deficiencia de proteínas localizadas en las mitocondrias e involucradas en el metabolismo; spontaneously occuring or inherited disorder that involves mitochondrial dysfunction; Erkrankung im Energiestoffwechsel; tauteja joissa ilmenee jokin mitokondrion toimintahäiriö; mitocondropatia; citopatia mitocondrial; mitocondropatía; enfermedad metabólica mitocondrial; enfermedad mitocondrial del metabolismo; mitocondropatia; enfermedad metabolica mitocondrial; Patología mitocondrial; mitochondropathie; mitohondrijsko bobolenje; mitohondrijska motnja; mitochondrial metabolism disease; Mitochondrial genetic disorders; Mitochondrial disease; mitochondrial diseases; mitokondriopati; 线粒体疾病; 線粒體疾病; 線粒體疾病</nowiki>
mitochondrial disease 
spontaneously occuring or inherited disorder that involves mitochondrial dysfunction
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Instance of
  • developmental defect during embryogenesis
  • designated intractable/rare disease
  • class of disease
Subclass of
  • inherited metabolic disorder
  • mtDNA transmission
  • developmental anomaly of metabolic origin
  • inborn disorder of energy metabolism
Authority file
Wikidata Q935710
NL CR AUT ID:
National Library of Spain SpMaBN ID (BNE v1.0):
BabelNet ID:
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Subcategories

This category has the following 11 subcategories, out of 11 total.

 

  • CT images of mitochondrial diseases (1 C)
  • Histopathology of mitochondrial diseases (3 C)
  • MRI of mitochondrial diseases (1 C, 1 F)
  • SVG mitochondrial diseases (1 F)
  • Ultrasound images of mitochondrial diseases (1 C)
  • Videos of mitochondrial diseases (29 F)

K

  • Kearns-Sayre syndrome (7 F)

L

  • Leigh syndrome (1 C, 1 F)

M

  • MELAS syndrome (3 C)
  • Mitochondrial myopathy (1 C, 11 F)

W

  • Wolfram syndrome (1 C, 3 F)

Media in category "Mitochondrial diseases"

The following 15 files are in this category, out of 15 total.

  • 12967 2022 3685 Fig1 HTML.webp 685 × 550; 55 KB
  • 13311 2018 674 Fig1 HTML (1).webp 685 × 480; 65 KB
  • 2014 Quijada-Fraile et al -- Фолиниевая кислота при синдроме Кернса-Сейра.pdf 1,239 × 1,752, 15 pages; 1.46 MB
  • Autophagy monocite.jpg 1,200 × 1,474; 287 KB
  • Fgene-09-00669-g003.jpg 1,084 × 552; 308 KB
  • Figure 3 - Pedigree of family with POLG mutations (Korinthenberg et al 2021).png 715 × 369; 30 KB
  • Herència de l'al·lel mutant.png 845 × 385; 15 KB
  • Human wild-type full-length tau accumulation disrupts mitochondrial dynamics and the functions via increasing mitofusins Fig 1.jpg 787 × 780; 322 KB
  • Maternal Inheritance - mitochondrial DNA.png 2,528 × 1,784; 166 KB
  • Maternale Vererbung - mitochondriale DNA.png 2,528 × 1,924; 176 KB
  • Mitochondrial disease.png 3,395 × 1,986; 634 KB
  • Mitochondrial DNA and diseases.png 1,855 × 1,537; 108 KB
  • Mitophagy purkinje cell (cropped).jpg 171 × 209; 12 KB
  • Mitophagy purkinje cell.jpg 600 × 617; 142 KB
  • Заболевание с чертами синдрома Альперса и МНГИЭ, нарушением переноса фолатов в СМЖ, и необычной мутацией гена POLG.pdf 1,239 × 1,752, 15 pages; 1.3 MB
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