Molekulargenetik

Erkrankungen Gene

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Anforderungsbeleg

AFB Molekulargenetik

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Alpers Huttenlocher Syndrom

POLG

Chronisch progressive externe Ophthalmoplegie (CPEO)

MT-TA, MT-TI, MT-TL1, MT-TL2, MT-TN, POLG

Diabetes-Deafness Syndrom

MT-RNR1, MT-TE, MT-TI, MT-TK, MT-TL1, MT-TS2

Kearns-Sayre Syndrom

MT-TL2

Leber ́sche hereditäre Optikusneuropathie (LHON)

MT-ND1, MT-ND4, MT-ND6

Leigh Syndrom

MT-ATP6, MT-ND3, MT-ND5, MT-ND6, MT-TA, MT-TE, MT-TG, MT-TK, MT-TL1, MT-TW

MELAS

MT-TL1

MERRF

MT-TK, MT-TL1

Mitochondriale Myopathie

MT-TE, MT-TH, MT-TK, MT-TL1, MT-TL2, MT-TP, MT-TS2, MT-TT

NARP

MT-ATP6

Taubheit, Aminoglycosid-induziert