Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Back [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.000422561
GER [NCBI] 0.000102676
EN1 [NCBI] 7.10677e-06
OCA2 [NCBI] 6.93717e-06
MYO5A [NCBI] 6.60783e-06
FABP2 [NCBI] 6.57109e-06
KRT10 [NCBI] 6.08178e-06
ATXN3 [NCBI] 5.6929e-06
FAAH [NCBI] 5.44243e-06
TYRP1 [NCBI] 5.32695e-06
MITF [NCBI] 5.05187e-06
BRAF [NCBI] 4.80219e-06
MSH2 [NCBI] 4.67024e-06
GJB2 [NCBI] 4.42403e-06
MLH1 [NCBI] 4.34933e-06
MLL [NCBI] 4.28168e-06
CTNNB1 [NCBI] 3.01849e-06
EPO [NCBI] 2.83544e-06
MS [NCBI] 2.50506e-06
EGFR [NCBI] 2.44941e-06
ACHE [NCBI] 2.43816e-06



OMIM


 OMIM Link Information
gain		 01
striae distensae, familial [NCBI] 0.00158502
alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality [NCBI] 0.0012742
lethal congenital contracture syndrome 1 [NCBI] 0.00108094
IS1 [NCBI] 0.000953538
facial ectodermal dysplasia [NCBI] 0.000835024
pena-shokeir syndrome, type i [NCBI] 0.000614097
MTS [NCBI] 0.000474418
halo nevi [NCBI] 0.000235516
GPHN [NCBI] 0.000196245
DFSP [NCBI] 0.000192396
hypertrichosis, anterior cervical [NCBI] 0.000181427
hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy [NCBI] 0.000181427
schwannomatosis [NCBI] 0.000158956
amyloidosis, primary cutaneous [NCBI] 0.000126207
EBR1 [NCBI] 0.000119118
ED1 [NCBI] 9.87094e-05
glycogen storage disease ii [NCBI] 8.87068e-05
FABP2 [NCBI] 5.17116e-05
FAAH [NCBI] 3.33036e-05
ABP1 [NCBI] 3.22323e-05
EPO [NCBI] 1.44618e-05
ACHE [NCBI] 1.16136e-05



Database Center for Life Science