Category:Mitochondrial diseases

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Radiology: Ultrasound · Computed tomography · Magnetic resonance | Anatomical pathology: Histopathology | File format: SVG · Video recording |

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
Q935710 NL CR AUT ID: ph893660 National Library of Spain ID: XX4670170 BabelNet ID: 00839112n
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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 (6 F)

L

Leigh syndrome‎ (1 C, 1 F)

M

MELAS syndrome‎ (3 C)
Mitochondrial myopathy‎ (1 C, 10 F)

W

Wolfram syndrome‎ (1 C, 3 F)

Media in category "Mitochondrial diseases"

The following 12 files are in this category, out of 12 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
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 DNA and diseases.png 1,855 × 1,537; 108 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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