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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cerebral Amyloid Angiopathy, Familial [NCBI]

Gene


 Gene Link Information
Gain		 01
APP [NCBI] 6.99316e-05
ITM2B [NCBI] 2.43744e-05
LRPAP1 [NCBI] 1.17939e-05
SERPINI1 [NCBI] 1.00617e-05
NOTCH3 [NCBI] 7.7228e-06
PRNP [NCBI] 6.81953e-06
EGR1 [NCBI] 6.78158e-06
MAPT [NCBI] 6.01734e-06
LIF [NCBI] 5.74536e-06
CST3 [NCBI] 5.42762e-06
ACHE [NCBI] 4.64537e-06
CD68 [NCBI] 4.49225e-06
MBP [NCBI] 4.26223e-06
APOE [NCBI] 3.34667e-06



OMIM


 OMIM Link Information
gain		 01
amyloidosis vi [NCBI] 0.000868156
HCHWAD [NCBI] 0.000309858
amyloidosis, cerebroarterial, hereditary, iowa type [NCBI] 0.000110446
APP [NCBI] 9.76002e-05
SDC2 [NCBI] 4.15507e-05
AD [NCBI] 2.75965e-05
FTD [NCBI] 2.28628e-05
ACHE [NCBI] 2.05458e-05
MBP [NCBI] 1.86016e-05
APOE [NCBI] 1.66341e-05



Database Center for Life Science