Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	5-Hydroxytryptophan	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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