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MeSH keywords -> Related genes, diseases (OMIM)


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01 Olfaction Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
ANIC [NCBI] 0.000438875
KAL1 [NCBI] 0.000221549
FGFR1 [NCBI] 7.06667e-05
GNRHR [NCBI] 2.90575e-05
KISS1R [NCBI] 2.90575e-05
APOE [NCBI] 2.62651e-05
OR1D2 [NCBI] 1.41473e-05
ADCY4 [NCBI] 1.32489e-05
PAX6 [NCBI] 1.24885e-05
XG [NCBI] 1.15987e-05
PRKAR1B [NCBI] 1.15987e-05
NELF [NCBI] 1.13527e-05
PROKR2 [NCBI] 1.09465e-05
PARK2 [NCBI] 1.00085e-05
PROK2 [NCBI] 9.99877e-06
PRL [NCBI] 9.88257e-06
KCNA3 [NCBI] 9.71217e-06
GNRH1 [NCBI] 9.62639e-06
OMP [NCBI] 9.39216e-06
CEP290 [NCBI] 9.18616e-06
SORL1 [NCBI] 9.06144e-06
BBS1 [NCBI] 8.94519e-06
MS [NCBI] 7.68417e-06
WFDC5 [NCBI] 7.61068e-06
FGF8 [NCBI] 7.48675e-06
KISS1 [NCBI] 7.04692e-06
VKORC1 [NCBI] 7.02857e-06
GBA [NCBI] 6.58189e-06
FGFR2 [NCBI] 5.79966e-06
LRRK2 [NCBI] 5.73064e-06
ATXN3 [NCBI] 5.72221e-06
GNAS [NCBI] 5.6725e-06
FGFR3 [NCBI] 4.23384e-06
MAPT [NCBI] 3.97951e-06
HTT [NCBI] 3.48729e-06
SNCA [NCBI] 3.21923e-06
BDNF [NCBI] 2.7726e-06
TH [NCBI] 2.70426e-06
CD68 [NCBI] 2.52122e-06
CASP3 [NCBI] 1.34777e-06
PTH [NCBI] 1.02608e-06



OMIM


 OMIM Link Information
gain		 01
anosmia, congenital [NCBI] 0.00490684
johnson neuroectodermal syndrome [NCBI] 0.00423362
musk, inability to smell [NCBI] 0.0020881
KAL1 [NCBI] 0.00124948
KAL2 [NCBI] 0.00123721
isovaleric acid, inability to smell [NCBI] 0.000377979
MBS [NCBI] 0.00033954
hypogonadotropic hypogonadism [NCBI] 0.000325414
androstenone, ability to smell [NCBI] 0.000251552
ichthyosis, x-linked [NCBI] 0.000218588
FGFR1 [NCBI] 0.000164351
GNAL [NCBI] 0.00014301
neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia [NCBI] 0.000125563
kallmann syndrome with spastic paraplegia [NCBI] 0.000125563
anosmia for isobutyric acid [NCBI] 0.000125563
retinitis pigmentosa inversa with deafness [NCBI] 0.000125563
brachytelephalangy with characteristic facies and kallmann syndrome [NCBI] 0.000125563
arhinia, choanal atresia, and microphthalmia [NCBI] 9.46218e-05
CNGA2 [NCBI] 8.08766e-05
ADCY4 [NCBI] 8.08766e-05
ADCY2 [NCBI] 8.08766e-05
ADCY3 [NCBI] 8.08766e-05
eunuchoidism, familial hypogonadotropic [NCBI] 7.67499e-05
CDPX1 [NCBI] 6.218e-05
leopard syndrome 1 [NCBI] 5.41573e-05
AN2 [NCBI] 4.61212e-05
GNRH1 [NCBI] 4.10106e-05
MDD [NCBI] 4.05329e-05
OMP [NCBI] 3.962e-05
AHO [NCBI] 3.54667e-05
BBS [NCBI] 3.16412e-05
PAX6 [NCBI] 3.06539e-05
PD [NCBI] 2.87597e-05
PRL [NCBI] 1.80722e-05
apnea, obstructive sleep [NCBI] 1.57561e-05
SLC6A3 [NCBI] 1.45009e-05
CF [NCBI] 1.30614e-05
APOE [NCBI] 1.07798e-05
FTD [NCBI] 9.68926e-06
BDNF [NCBI] 4.25405e-06
TH [NCBI] 3.50928e-06
PTH [NCBI] 9.35409e-08
AD [NCBI] 1.64823e-08



Database Center for Life Science