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Descriptor English: Mitochondrial Diseases
Descriptor Spanish: Enfermedades Mitocondriales
Descriptor enfermedades mitocondriales
Entry term(s) deficiencias de fosforilación oxidativa
deficiencias mitocondriales de la cadena de transporte de electrones
enfermedad mitocondrial
Scope note: Enfermedades causadas por un funcionamiento anómalo de la MITOCONDRIA, que puede deberse a mutaciones, adquiridas o heredadas, en el ADN mitocondrial o en genes del núcleo encargados de codificar componentes mitocondriales. Estas enfermedades tambien pueden ser resultado de disfunciones mitocondriales adquiridas, derivadas de efectos adversos de drogas, infecciones u otras causas ambientales.
Descriptor Portuguese: Doenças Mitocondriais
Descriptor French: Maladies mitochondriales
Entry term(s): Deficiencies, Oxidative Phosphorylation
Deficiencies, Respiratory Chain
Deficiency, Oxidative Phosphorylation
Deficiency, Respiratory Chain
Disease, Mitochondrial
Disorder, Mitochondrial
Disorders, Mitochondrial
Electron Transport Chain Deficiencies, Mitochondrial
Mitochondrial Disease
Mitochondrial Disorder
Mitochondrial Disorders
Mitochondrial Electron Transport Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies
Oxidative Phosphorylation Deficiencies
Oxidative Phosphorylation Deficiency
Phosphorylation Deficiencies, Oxidative
Phosphorylation Deficiency, Oxidative
Respiratory Chain Deficiencies, Mitochondrial
Respiratory Chain Deficiency
Tree number(s): C18.452.660
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D028361
Scope note: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
Annotation: general or unspecified; prefer specifics
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Mitochondria (1987-2001)
Mitochondrial Myopathies (1992-2001)
Public MeSH Note: 2002; see MITOCHONDRIAL MYOPATHIES 2000-2001
History Note: 2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
Entry Version: MITOCHONDRIAL DIS
DeCS ID: 36033
Unique ID: D028361
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2002/01/01
Date of Entry: 2001/08/03
Mitochondrial Diseases - Preferred
Concept UI M0335637
Scope note Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
Preferred term Mitochondrial Diseases
Entry term(s) Disease, Mitochondrial
Disorder, Mitochondrial
Disorders, Mitochondrial
Mitochondrial Disease
Mitochondrial Disorder
Mitochondrial Disorders
Oxidative Phosphorylation Deficiencies - Narrower
Concept UI M0382031
Preferred term Oxidative Phosphorylation Deficiencies
Entry term(s) Deficiencies, Oxidative Phosphorylation
Deficiency, Oxidative Phosphorylation
Oxidative Phosphorylation Deficiency
Phosphorylation Deficiencies, Oxidative
Phosphorylation Deficiency, Oxidative
Respiratory Chain Deficiencies, Mitochondrial - Narrower
Concept UI M0382030
Preferred term Respiratory Chain Deficiencies, Mitochondrial
Entry term(s) Deficiencies, Respiratory Chain
Deficiency, Respiratory Chain
Mitochondrial Respiratory Chain Deficiencies
Respiratory Chain Deficiency
Electron Transport Chain Deficiencies, Mitochondrial - Narrower
Concept UI M0387124
Preferred term Electron Transport Chain Deficiencies, Mitochondrial
Entry term(s) Mitochondrial Electron Transport Chain Deficiencies



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