MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Flavin-Adenine Dinucleotide
[NCBI]
Gene
Gene
Link
Information
Gain
01
POR
[NCBI]
1.92004e-05
XDH
[NCBI]
1.44101e-05
NOS1
[NCBI]
1.01696e-05
DMGDH
[NCBI]
6.88938e-06
MTRR
[NCBI]
6.3638e-06
DAO
[NCBI]
5.78385e-06
CYBB
[NCBI]
5.4498e-06
GSR
[NCBI]
5.34723e-06
MAOB
[NCBI]
5.0902e-06
NDOR1
[NCBI]
4.3008e-06
MAOA
[NCBI]
4.26843e-06
L2HGDH
[NCBI]
4.21815e-06
MICAL1
[NCBI]
4.02709e-06
NQO2
[NCBI]
3.81005e-06
PRODH
[NCBI]
3.75905e-06
DLD
[NCBI]
3.72756e-06
CYB5R3
[NCBI]
3.58134e-06
LDHD
[NCBI]
3.42168e-06
CYCS
[NCBI]
3.35678e-06
CHM
[NCBI]
3.17686e-06
PPOX
[NCBI]
3.11511e-06
AIFM1
[NCBI]
2.70503e-06
CYBA
[NCBI]
2.45175e-06
PSEN1
[NCBI]
2.44895e-06
MICALCL
[NCBI]
2.38486e-06
PSEN2
[NCBI]
2.22245e-06
MICALL2
[NCBI]
2.12769e-06
SLC25A32
[NCBI]
2.12769e-06
PAOX
[NCBI]
2.08934e-06
DAK
[NCBI]
2.08934e-06
MICAL2
[NCBI]
2.05581e-06
PLXNA4
[NCBI]
2.02603e-06
KMO
[NCBI]
1.99923e-06
MICALL1
[NCBI]
1.99923e-06
CPZ
[NCBI]
1.97488e-06
ERO1LB
[NCBI]
1.95256e-06
GPD1
[NCBI]
1.95256e-06
MICAL3
[NCBI]
1.95256e-06
AIFM2
[NCBI]
1.93197e-06
SARDH
[NCBI]
1.87827e-06
GPD2
[NCBI]
1.84766e-06
QSOX1
[NCBI]
1.84766e-06
PIPOX
[NCBI]
1.83358e-06
SQLE
[NCBI]
1.83358e-06
DHCR24
[NCBI]
1.80746e-06
GCDH
[NCBI]
1.7953e-06
FDXR
[NCBI]
1.7953e-06
IMMT
[NCBI]
1.77252e-06
DHFR
[NCBI]
1.73245e-06
CRMP1
[NCBI]
1.71394e-06
ERO1L
[NCBI]
1.71394e-06
SEMA3B
[NCBI]
1.66592e-06
CRY1
[NCBI]
1.66592e-06
CYP11B1
[NCBI]
1.57912e-06
ACADM
[NCBI]
1.57912e-06
FMO3
[NCBI]
1.56874e-06
AOF2
[NCBI]
1.50962e-06
DAOA
[NCBI]
1.50557e-06
NOS2
[NCBI]
1.48278e-06
DHDH
[NCBI]
1.46467e-06
TXNRD1
[NCBI]
1.43843e-06
DPYD
[NCBI]
1.42031e-06
HBG2
[NCBI]
1.3468e-06
PANK2
[NCBI]
1.29105e-06
GPX1
[NCBI]
1.11876e-06
CYP1A2
[NCBI]
1.09285e-06
KCNJ8
[NCBI]
1.08039e-06
SHH
[NCBI]
9.26312e-07
ABCG2
[NCBI]
8.85811e-07
COMT
[NCBI]
7.48126e-07
BACE1
[NCBI]
7.35082e-07
MTHFR
[NCBI]
6.88536e-07
NOS3
[NCBI]
5.7298e-07
CCK
[NCBI]
4.43529e-07
EGF
[NCBI]
1.90105e-07
OMIM
OMIM
Link
Information
gain
01
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
[NCBI]
0.00033803
XDH
[NCBI]
0.000221419
MADD
[NCBI]
0.000214797
DAO
[NCBI]
0.000195719
CGD
[NCBI]
0.000184653
PRODH
[NCBI]
0.000147787
desmosterolosis
[NCBI]
0.000132807
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
[NCBI]
0.000125733
ACADM
[NCBI]
0.000125482
l-2-hydroxyglutaric aciduria
[NCBI]
0.000120349
ABS
[NCBI]
0.000109212
d-bifunctional protein deficiency
[NCBI]
0.000105192
CDPX2
[NCBI]
0.000103996
GSR
[NCBI]
0.000102003
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i
[NCBI]
9.61957e-05
acyl-coa dehydrogenase, medium-chain, deficiency of
[NCBI]
9.3118e-05
porphyria variegata
[NCBI]
7.59051e-05
MTHFR
[NCBI]
6.33924e-05
SLOS
[NCBI]
5.48506e-05
IVD
[NCBI]
4.92602e-05
flavoprotein oxidoreductase mical3
[NCBI]
4.42462e-05
methemoglobinemia due to deficiency of methemoglobin reductase
[NCBI]
4.11654e-05
flavoprotein oxidoreductase mical2
[NCBI]
3.6824e-05
NICAL
[NCBI]
3.6824e-05
NDOR1
[NCBI]
3.40234e-05
FLAD1
[NCBI]
3.40234e-05
L2HGDH
[NCBI]
3.08535e-05
SLC25A32
[NCBI]
3.08535e-05
DHCR24
[NCBI]
2.97767e-05
ETFDH
[NCBI]
2.88814e-05
RAC2
[NCBI]
2.68505e-05
PDCD8
[NCBI]
2.53871e-05
FMO1
[NCBI]
2.5384e-05
TYMS
[NCBI]
2.28788e-05
ACADVL
[NCBI]
2.2745e-05
HSD17B4
[NCBI]
2.2745e-05
NOS1
[NCBI]
2.09914e-05
CYBB
[NCBI]
2.01326e-05
CRY1
[NCBI]
2.01326e-05
PPOX
[NCBI]
1.99764e-05
ACP1
[NCBI]
1.96774e-05
FMO3
[NCBI]
1.9534e-05
ACADS
[NCBI]
1.85094e-05
MTR
[NCBI]
1.50653e-05
DHFR
[NCBI]
9.32927e-06
EGF
[NCBI]
4.6809e-06
COMT
[NCBI]
4.19114e-06
CCK
[NCBI]
1.46769e-09
Database Center for Life Science