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MeSH keywords -> Related genes, diseases (OMIM)


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01 Phenylketonurias [NCBI]


Gene


Gene Link Information
Gain
01
PAH [NCBI] 0.00458953
QDPR [NCBI] 0.000101749
PCBD1 [NCBI] 9.26551e-05
PTS [NCBI] 7.28159e-05
SPR [NCBI] 3.9107e-05
MAOB [NCBI] 1.1782e-05
GCH1 [NCBI] 1.14183e-05
ARSE [NCBI] 6.80132e-06
HNF1B [NCBI] 5.48553e-06
HNF1A [NCBI] 5.21406e-06
CAT [NCBI] 4.56224e-06
S100B [NCBI] 4.49774e-06
GALT [NCBI] 4.47037e-06
ASCL1 [NCBI] 4.26662e-06
SLC3A1 [NCBI] 4.08578e-06
PROC [NCBI] 3.5322e-06
MBP [NCBI] 3.36399e-06
CYP21A2 [NCBI] 3.07944e-06
KRT14 [NCBI] 3.00312e-06
MTRR [NCBI] 2.97157e-06
MTR [NCBI] 2.92044e-06
G6PD [NCBI] 2.80216e-06
DMD [NCBI] 2.71443e-06
GHRL [NCBI] 2.44464e-06
NEFH [NCBI] 2.09564e-06
MYOC [NCBI] 2.06798e-06
FOLH1 [NCBI] 2.06252e-06
ACHE [NCBI] 1.79647e-06
BTK [NCBI] 1.63186e-06
IGF1 [NCBI] 1.33378e-06
CTSL1 [NCBI] 1.20258e-06
TTR [NCBI] 1.13906e-06
APOB [NCBI] 8.80216e-07
FMR1 [NCBI] 6.23652e-07
PRL [NCBI] 3.76712e-07
TH [NCBI] 2.26448e-07
MTHFR [NCBI] 1.90862e-07
CFTR [NCBI] 1.86613e-07
APOE [NCBI] 5.85173e-08
GFAP [NCBI] 6.96334e-14




OMIM


OMIM Link Information
gain
01
phenylketonuria [NCBI] 0.0140807
methionine malabsorption syndrome [NCBI] 0.00222949
phenylketonuria ii [NCBI] 0.00121156
folic acid, transport defect involving [NCBI] 0.000798231
PTS [NCBI] 0.000677033
gtp cyclohydrolase i deficiency [NCBI] 0.000470678
SPR [NCBI] 0.000170681
maple syrup urine disease [NCBI] 0.000127806
SC [NCBI] 0.000113311
methylmalonyl-coa epimerase deficiency [NCBI] 0.000104833
hyperphenylalaninemia with primapterinuria [NCBI] 0.000104833
PCBD1 [NCBI] 9.16715e-05
MRT1 [NCBI] 8.69446e-05
hyperbilirubinemia, transient familial neonatal [NCBI] 8.69446e-05
elliptocytosis, rhesus-unlinked type [NCBI] 8.49166e-05
cystathioninuria [NCBI] 7.86743e-05
GAL3ST1 [NCBI] 7.15044e-05
histidinemia [NCBI] 6.65411e-05
RP1 [NCBI] 6.42765e-05
GCH1 [NCBI] 5.39232e-05
SDS [NCBI] 4.68636e-05
CF [NCBI] 4.62629e-05
HGD [NCBI] 2.6944e-05
ALD [NCBI] 2.29949e-05
aspartylglucosaminuria [NCBI] 1.91537e-05
ADIPOQ [NCBI] 1.80024e-05
panencephalitis, subacute sclerosing [NCBI] 1.75268e-05
GFAP [NCBI] 1.65397e-05
SPTA1 [NCBI] 1.33485e-05
HNF1A [NCBI] 1.30455e-05
PRL [NCBI] 1.20217e-05
ACADM [NCBI] 9.63382e-06
MYOC [NCBI] 9.00626e-06
homocystinuria [NCBI] 8.05109e-06
TH [NCBI] 5.15986e-06
AKR1B1 [NCBI] 5.13288e-06
MAG [NCBI] 3.44926e-06
CAT [NCBI] 1.55177e-06
ACHE [NCBI] 3.45638e-07
G6PD [NCBI] 5.12684e-08
TTR [NCBI] 3.10476e-08
APOB [NCBI] 1.26371e-08
MBP [NCBI] 5.86065e-09




Database Center for Life Science