Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 5-Hydroxytryptophan [NCBI]

Gene


 Gene Link Information
Gain		 01
PRL [NCBI] 5.09668e-05
TRH [NCBI] 1.09793e-05
TH [NCBI] 7.28199e-06
DDC [NCBI] 4.9776e-06
PTS [NCBI] 3.90239e-06
TPH2 [NCBI] 3.38132e-06
COMT [NCBI] 2.0664e-06
ADA [NCBI] 1.98302e-06
SLC6A4 [NCBI] 1.87305e-06
SLC18A1 [NCBI] 1.84331e-06
SLC26A6 [NCBI] 1.78266e-06
PCBD1 [NCBI] 1.52779e-06
SLC18A2 [NCBI] 1.46432e-06
TPH1 [NCBI] 1.42297e-06
MAOA [NCBI] 1.22764e-06
HDC [NCBI] 1.15822e-06
MB [NCBI] 1.03769e-06
GRM5 [NCBI] 9.9228e-07
AVP [NCBI] 5.60411e-07
VIP [NCBI] 5.60338e-07
CCK [NCBI] 5.38859e-07
NPY [NCBI] 4.65919e-07
PTH [NCBI] 4.20945e-07
TNF [NCBI] 2.41092e-07



OMIM


 OMIM Link Information
gain		 01
PRL [NCBI] 0.000454459
aromatic l-amino acid decarboxylase deficiency [NCBI] 0.000147714
pheochromocytoma [NCBI] 0.000122682
hyperekplexia, hereditary [NCBI] 0.000122682
PTS [NCBI] 0.0001178
neuraminidase deficiency [NCBI] 9.85042e-05
MEN2A [NCBI] 9.55008e-05
DDC [NCBI] 8.02753e-05
GTS [NCBI] 7.18891e-05
TH [NCBI] 4.22305e-05
MDD [NCBI] 4.19645e-05
HTR2B [NCBI] 3.24413e-05
TPH2 [NCBI] 2.52086e-05
TPH1 [NCBI] 2.41375e-05
HTR2A [NCBI] 2.22526e-05
phenylketonuria ii [NCBI] 2.1226e-05
CSTB [NCBI] 2.03669e-05
COMT [NCBI] 1.52022e-05
ADA [NCBI] 1.04999e-05
HDC [NCBI] 8.29508e-06
CRH [NCBI] 8.17364e-06
SLC6A4 [NCBI] 7.81014e-06
MB [NCBI] 6.14939e-06
ADCYAP1 [NCBI] 4.67089e-06
TNF [NCBI] 4.13176e-06
PTH [NCBI] 4.55481e-07
NPY [NCBI] 1.42509e-07
VIP [NCBI] 5.90182e-08
CCK [NCBI] 1.1977e-08
AVP [NCBI] 4.83309e-09



Database Center for Life Science