MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Sulfatases
[NCBI]
Gene
Gene
Link
Information
Gain
01
ARSC2
[NCBI]
0.000516462
STSP
[NCBI]
0.000216972
SUMF1
[NCBI]
9.0027e-05
STS
[NCBI]
3.30816e-05
SUMF2
[NCBI]
2.27926e-05
GNS
[NCBI]
2.02497e-05
ARSB
[NCBI]
1.30096e-05
SULF1
[NCBI]
1.09247e-05
SULF2
[NCBI]
9.18086e-06
ARSA
[NCBI]
7.1172e-06
XG
[NCBI]
6.56781e-06
GALNS
[NCBI]
5.47378e-06
ITPR1
[NCBI]
5.25716e-06
ARSJ
[NCBI]
4.88872e-06
ARSK
[NCBI]
4.88872e-06
ARSI
[NCBI]
4.88872e-06
ARSG
[NCBI]
4.58543e-06
TXNDC4
[NCBI]
4.14163e-06
SGSH
[NCBI]
3.99599e-06
IDS
[NCBI]
3.20567e-06
NAGA
[NCBI]
3.09105e-06
G6PD
[NCBI]
3.08077e-06
ARSH
[NCBI]
2.89329e-06
SULT1A1
[NCBI]
2.78539e-06
PSAP
[NCBI]
2.63048e-06
NOG
[NCBI]
2.17983e-06
ARSF
[NCBI]
2.12521e-06
ARSD
[NCBI]
2.12521e-06
PAPSS2
[NCBI]
1.95009e-06
CA13
[NCBI]
1.95009e-06
PAPSS1
[NCBI]
1.8758e-06
PDIA2
[NCBI]
1.80499e-06
ACO2
[NCBI]
1.72038e-06
SULT1E1
[NCBI]
1.67851e-06
OLIG1
[NCBI]
1.67851e-06
GSTT2
[NCBI]
1.54195e-06
SDC2
[NCBI]
1.37982e-06
HS3ST5
[NCBI]
1.35334e-06
LMAN1
[NCBI]
1.32511e-06
SHOX
[NCBI]
1.30911e-06
VKORC1
[NCBI]
1.09641e-06
CYP19A1
[NCBI]
1.0921e-06
TGFBI
[NCBI]
1.07712e-06
CD99
[NCBI]
1.04301e-06
FGF2
[NCBI]
1.01155e-06
TFF1
[NCBI]
9.25676e-07
OSM
[NCBI]
8.96451e-07
CTNNB1
[NCBI]
5.25057e-07
TGFB1
[NCBI]
4.85216e-07
ACHE
[NCBI]
3.98797e-07
TNF
[NCBI]
1.59644e-07
OMIM
OMIM
Link
Information
gain
01
MSD
[NCBI]
0.00480733
metachromatic leukodystrophy
[NCBI]
0.00319068
ichthyosis, x-linked
[NCBI]
0.00228357
mucopolysaccharidosis type iiid
[NCBI]
0.000966038
metachromatic leukodystrophy due to saposin b deficiency
[NCBI]
0.000696822
mucopolysaccharidosis type vi
[NCBI]
0.000560959
mucopolysaccharidosis type viii
[NCBI]
0.000442027
ARSB
[NCBI]
0.000341229
GNS
[NCBI]
0.000327813
mucopolysaccharidosis type iiia
[NCBI]
0.000243004
mucopolysaccharidosis type ii
[NCBI]
0.000242268
SUMF1
[NCBI]
0.000190095
CDPX1
[NCBI]
0.000175919
mucopolysaccharidosis type iva
[NCBI]
0.000154293
ARSA
[NCBI]
0.000134268
amish infantile epilepsy syndrome
[NCBI]
0.000115556
ichthyosis and male hypogonadism
[NCBI]
0.000115556
morquio syndrome, nonkeratosulfate-excreting type
[NCBI]
0.000115556
CF
[NCBI]
0.000111392
ARSJ
[NCBI]
8.17036e-05
ARSK
[NCBI]
8.17036e-05
ARSI
[NCBI]
8.17036e-05
sulfatase-modifying factor 2
[NCBI]
8.17036e-05
DMC
[NCBI]
7.58539e-05
NCIE1
[NCBI]
7.33523e-05
ISS
[NCBI]
7.33523e-05
ichthyosis vulgaris
[NCBI]
6.90665e-05
morquio syndrome b
[NCBI]
6.54819e-05
SGSH
[NCBI]
5.0196e-05
CD99
[NCBI]
5.0196e-05
mucopolysaccharidosis type vii
[NCBI]
4.7511e-05
hurler syndrome
[NCBI]
4.08851e-05
ARSH
[NCBI]
4.08314e-05
ARSC2
[NCBI]
4.08314e-05
KAL1
[NCBI]
3.92804e-05
mucolipidosis ii
[NCBI]
3.71534e-05
PSAP
[NCBI]
3.5262e-05
methemoglobinemia due to deficiency of methemoglobin reductase
[NCBI]
3.43743e-05
ARSG
[NCBI]
3.06111e-05
SULF2
[NCBI]
3.06111e-05
MIC2Y
[NCBI]
2.74437e-05
SULF1
[NCBI]
2.74437e-05
XG
[NCBI]
2.29131e-05
ACO2
[NCBI]
2.29131e-05
fabry disease
[NCBI]
2.24582e-05
NAGA
[NCBI]
2.11941e-05
tay-sachs disease, ab variant
[NCBI]
1.88615e-05
OA1
[NCBI]
1.84106e-05
SHOX
[NCBI]
1.64532e-05
GLB1
[NCBI]
1.57605e-05
TNF
[NCBI]
1.51496e-05
neuraminidase deficiency with beta-galactosidase deficiency
[NCBI]
1.47094e-05
VEGF
[NCBI]
1.36626e-05
CYP19A1
[NCBI]
1.30192e-05
CCL2
[NCBI]
1.2186e-05
G6PD
[NCBI]
1.2097e-05
ABCC2
[NCBI]
1.0568e-05
HEMB
[NCBI]
7.91122e-06
SDC2
[NCBI]
5.69072e-06
ACHE
[NCBI]
2.16726e-06
KLK3
[NCBI]
1.73273e-06
Database Center for Life Science