- mitochondrial disease
- Биология: митохондриальное заболевание (группа наследственных заболеваний, связанных с дефектами в работе митохондрий)
Универсальный англо-русский словарь. Академик.ру. 2011.
mitochondrial disease
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Mitochondrial disease — Classification and external resources Micrograph showing ragged red fibres, a finding seen in mitochondrial diseases. Muscle biopsy. Gomori trichrome stain … Wikipedia
Mitochondrial disease — Mutations (changes) in the mitochondrial chromosome are responsible for a number of disorders including, for example: An eye disease called Leber s hereditary optic atrophy; A type of epilepsy called MERRF which stands for Myoclonus Epilepsy with … Medical dictionary
Mitochondrial myopathy — Classification and external resources Simplified structure of a typical mitochondrion ICD 10 G … Wikipedia
Mitochondrial neurogastrointestinal encephalopathy syndrome — Classification and external resources ICD 9 277.87 OMIM 603041 … Wikipedia
Mitochondrial encephalomyopathy — Classification and external resources ICD 9 277.87 MeSH D017237 A Mitochondr … Wikipedia
Mitochondrial DNA — Human mitochondrial DNA … Wikipedia
Mitochondrial inheritance — The inheritance of a trait encoded in the mitochondrial genome. Because of the oddities of mitochondria, mitochondrial inheritance does not obey the classic rules of genetics. Persons with a mitochondrial disease may be male or female but they… … Medical dictionary
Mitochondrial DNA — (mtDNA) is the DNA of the mitochondrion, a structure situated in the cytoplasm of the cell rather than in the nucleus (where all the other chromosomes are located). All mtDNA is inherited from the mother. There are 2 to 10 copies of the mtDNA… … Medical dictionary
Mitochondrial permeability transition — Mitochondrial permeability transition, or MPT, is an increase in the permeability of the mitochondrial membranes to molecules of less than 1500 Daltons in molecular weight. MPT results from opening of mitochondrial permeability transition pores,… … Wikipedia
Mitochondrial trifunctional protein deficiency — Classification and external resources OMIM 609015 DiseasesDB 34111 eMedi … Wikipedia
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes — Infobox Disease Name = Mitochondrial encephalomyopathy, lactic acidosis, and stroke like episodes Caption = DiseasesDB = 8254 ICD10 = ICD9 = ICDO = OMIM = 540000 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1406 MeshID = D017241… … Wikipedia
