Acquired Creutzfeldt-Jakob Disease
Watchlist
Retrieved
2021-01-23
Source
Trials
—
Genes
PRNP,
KRT73,
KLRC2,
ATF6,
HLA-DQB1,
H4C4,
SRD5A3,
TUBB2A,
MSL3P1,
CPED1,
SNORD3A,
ALDH1A1,
SNORA16B,
MTMR7,
CARD14,
PLCXD3,
MAPT,
SERPINF2,
RGS7,
C4BPA,
APOE,
ABCB6,
GH1,
PRDX2,
SNCA,
CSF2,
LAMC2,
GFAP,
PRND,
SPRN
PRNP,
KRT73,
KLRC2,
ATF6,
HLA-DQB1,
H4C4,
SRD5A3,
TUBB2A,
MSL3P1,
CPED1,
SNORD3A,
ALDH1A1,
SNORA16B,
MTMR7,
CARD14,
PLCXD3,
MAPT,
SERPINF2,
RGS7,
C4BPA,
APOE,
ABCB6,
GH1,
PRDX2,
SNCA,
CSF2,
LAMC2,
GFAP,
PRND,
SPRN,
ENO2,
CTSD,
AQP1,
AQP4,
CHI3L1,
APP,
RASA2,
NES,
CST7,
SUCLA2,
TSHZ1,
YWHAH,
DHX16,
RAB7A,
GRAP2,
RARB,
PTGS2,
ATXN2,
S100B,
AIMP2,
OPTN,
RAB9A,
ACHE,
AHSA1,
YWHAQ,
LINC01672,
FAS-AS1,
MT1IP,
ZBTB38,
CBLL2,
PRNT,
HECTD2,
TMEM171,
MINDY4,
ZIC4,
MAGT1,
MUL1,
MARK4,
ALG1,
TREM2,
PTGS1,
AATF,
POLDIP2,
RNF19A,
BACE1,
STMN2,
AHSP,
NRGN,
RELN,
CD68,
GRN,
GPI,
CYBB,
MAPK14,
CRYAB,
CRK,
ATF2,
CREB1,
CHIT1,
CHGB,
CHGA,
CFTR,
CD47,
HSPA4,
CBS,
CASP3,
TSPO,
BMP5,
BMP4,
ATF4,
ARF1,
AMT,
ALPP,
ALPI,
ALB,
AIF1,
HTT,
IAPP,
EIF2AK2,
MT1X,
MAPK3,
MAPK1,
ABCB1,
PGAM1,
PRKN,
ADAM10,
NPAS2,
NEFL,
MTNR1A,
COX2,
COX1,
MT3,
MT1L,
IL1A,
MT1M,
MT1JP,
MT1H,
MT1G,
MT1F,
MT1E,
MT1B,
MT1A,
MDH1,
MBP,
LY6E,
IL1B,
MTCO2P12
Registered!
A group of human prion diseases characterized by progressive, invariably fatal neurodegeneration resulting from accidental transmission of prions. The group comprises iatrogenic Creutzfeldt-Jakob disease (CJD), which results from transmission of CJD prions in the course of medical procedures or treatments, and variant CJD (transmission via consumption of products from prion-diseased cows or via blood transfusion from an affected individual).