Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Anticipation, Genetic [NCBI]

Gene


 Gene Link Information
Gain		 01
TERC [NCBI] 0.000668532
IBGC1 [NCBI] 0.000497921
ATXN2 [NCBI] 3.74843e-05
BMPR2 [NCBI] 3.6468e-05
DKC1 [NCBI] 2.525766e-05
SPAST [NCBI] 2.320198e-05
CACNA1A [NCBI] 2.060789e-05
BSN [NCBI] 1.729174e-05
MAB21L1 [NCBI] 1.710926e-05
MSH2 [NCBI] 1.35735e-05
VPS13A [NCBI] 1.342532e-05
KCNN3 [NCBI] 1.339703e-05
SIX5 [NCBI] 1.3374e-05
ATXN7 [NCBI] 1.336402e-05
ATN1 [NCBI] 1.319667e-05
ADORA2A [NCBI] 1.274038e-05
MS [NCBI] 1.248727e-05
HLA-DRA [NCBI] 1.208385e-05
TBP [NCBI] 1.104203e-05
APOE [NCBI] 1.002373e-05
ATXN1 [NCBI] 9.19703e-06
DMPK [NCBI] 8.06421e-06
TERT [NCBI] 7.76842e-06
PMP22 [NCBI] 7.60177e-06
PARK2 [NCBI] 6.77285e-06
BRCA2 [NCBI] 6.71807e-06
BRCA1 [NCBI] 5.8403e-06
JAK2 [NCBI] 5.79603e-06



OMIM


 OMIM Link Information
gain		 01
IBGC1 [NCBI] 0.001512887
aneurysm, intracranial berry, 1 [NCBI] 0.001368838
MAFD6 [NCBI] 0.001103669
DRPLA [NCBI] 0.000624965
CLL [NCBI] 0.000475923
SCA17 [NCBI] 0.000323515
dystrophia myotonica 1 [NCBI] 0.000274256
DM2 [NCBI] 0.000263808
SCA2 [NCBI] 0.000230966
TERC [NCBI] 0.0002050402
SMAX1 [NCBI] 0.0001852225
dyskeratosis congenita, autosomal dominant [NCBI] 0.000166076
myeloma, multiple [NCBI] 0.0001519965
SCA10 [NCBI] 0.000137124
camurati-engelmann disease [NCBI] 0.0001334274
hodgkin lymphoma [NCBI] 0.0001301579
SPG4 [NCBI] 0.0001180548
SPG3A [NCBI] 0.0001164888
SCA6 [NCBI] 0.000107264
HD [NCBI] 0.0001027579
SCA7 [NCBI] 0.0001021234
ATXN3 [NCBI] 9.87798e-05
DRPLA [NCBI] 9.29891e-05
ALS1 [NCBI] 9.06777e-05
lynch syndrome i [NCBI] 9.03528e-05
MSH2 [NCBI] 7.90774e-05
lymphoma, non-hodgkin, familial [NCBI] 7.73627e-05
TERT [NCBI] 6.82307e-05
RA [NCBI] 5.17882e-05
MJD [NCBI] 4.96593e-05
TTR [NCBI] 3.97731e-05
APOE [NCBI] 2.203181e-05
CRC [NCBI] 9.17096e-07



Database Center for Life Science