Search on: OXIDATIVE PHOSPHORYLATION DEFICIENCIES 
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Descriptor English:   Mitochondrial Diseases 
Descriptor Spanish:   Enfermedades Mitocondriales 
Descriptor Portuguese:   Doenças Mitocondriais 
Synonyms English:   Electron Transport Chain Deficiencies, Mitochondrial
Oxidative Phosphorylation Deficiencies
Respiratory Chain Deficiencies, Mitochondrial  
Tree Number:   C18.452.660
Definition English:   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. 
Indexing Annotation English:   GEN or unspecified; prefer specifics
History Note English:   2002; use MITOCHONDRIAL MYOPATHIES 2000-2001 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RA radiography
RI radionuclide imaging RT radiotherapy
RH rehabilitation SU surgery
TH therapy US ultrasonography
UR urine VE veterinary
VI virology  
Record Number:   36033 
Unique Identifier:   D028361 

Occurrence in VHL:
 

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