Molekulargenetik
Neurologische Erkrankungen
Anforderungsbeleg
AFB Molekulargenetik
CADASIL Syndrom
NOTCH3
Chorea Huntington
HTT
Chorea Huntington-like (HD-like)
DRPLA (ATN1), HD-like 1 (PRNP), HD-like 2 (JPH3), HD-like 4 (TBP)
Choreatiforme Bewegungsstörung
ADCY5, ARSA, DRPLA (ATN1), FRRS1L, FTL, GM2A, GNAO1, HD (HTT), HDlike (JPH3, JPH3, KCNA1, NKX2-1, PRNP, RNF216, SCA 1, SCA 2, SCA 3, SCA 6, SCA 7, TBP, VPS13A, XK
Creutzfeldt-Jacob-Krankheit (CJD)
PRNP