MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Arylsulfatases
[NCBI]
Gene
Gene
Link
Information
Gain
01
ARSC2
[NCBI]
0.000494854
HDHD1CP
[NCBI]
0.000243173
HDHD1BP
[NCBI]
0.000208465
STSP
[NCBI]
0.000208465
ARSE
[NCBI]
4.92324e-05
STS
[NCBI]
3.74977e-05
ARSD
[NCBI]
1.07332e-05
ARSB
[NCBI]
6.21787e-06
ARSA
[NCBI]
5.4152e-06
ARSF
[NCBI]
4.87817e-06
ARSG
[NCBI]
4.79502e-06
GNS
[NCBI]
4.38578e-06
SULF2
[NCBI]
4.38578e-06
SULF1
[NCBI]
4.05155e-06
GALNS
[NCBI]
3.6349e-06
SHOX
[NCBI]
3.20218e-06
FGFR3
[NCBI]
2.42065e-06
ARSJ
[NCBI]
2.32808e-06
ARSK
[NCBI]
2.32808e-06
ARSI
[NCBI]
2.32808e-06
HDHD1A
[NCBI]
2.12774e-06
ACP2
[NCBI]
1.9219e-06
SULT1B1
[NCBI]
1.85322e-06
ACO2
[NCBI]
1.82453e-06
SULT1E1
[NCBI]
1.78266e-06
IL1RN
[NCBI]
1.72611e-06
GPR143
[NCBI]
1.70865e-06
TPSAB1
[NCBI]
1.69714e-06
SLCO1B3
[NCBI]
1.61535e-06
SLC26A2
[NCBI]
1.56974e-06
CTCF
[NCBI]
1.55612e-06
CYP3A7
[NCBI]
1.54315e-06
KAL1
[NCBI]
1.4739e-06
PPOX
[NCBI]
1.47147e-06
NAGA
[NCBI]
1.46197e-06
PROC
[NCBI]
1.32604e-06
SULT1A1
[NCBI]
1.30974e-06
DNASE2B
[NCBI]
1.27403e-06
PSAP
[NCBI]
1.23252e-06
MGP
[NCBI]
1.21813e-06
SCP2
[NCBI]
1.20184e-06
CA9
[NCBI]
1.18899e-06
SOX9
[NCBI]
1.15971e-06
SRY
[NCBI]
1.13953e-06
PAH
[NCBI]
1.09028e-06
MATN1
[NCBI]
1.08571e-06
SELPLG
[NCBI]
1.05933e-06
ALB
[NCBI]
9.64061e-07
TTR
[NCBI]
9.36973e-07
G6PD
[NCBI]
8.36729e-07
PTHLH
[NCBI]
8.36073e-07
CYP3A4
[NCBI]
7.09492e-07
AFP
[NCBI]
6.12225e-07
MPO
[NCBI]
5.88703e-07
CCK
[NCBI]
5.38859e-07
OMIM
OMIM
Link
Information
gain
01
acroosteolysis with osteoporosis and changes in skull and mandible
[NCBI]
0.00277021
ichthyosis, x-linked
[NCBI]
0.0010406
metachromatic leukodystrophy
[NCBI]
0.000841062
MSD
[NCBI]
0.000398399
CDPX1
[NCBI]
0.000371061
ARSE
[NCBI]
0.000270212
mucolipidosis iiia
[NCBI]
0.000204383
mucopolysaccharidosis type vi
[NCBI]
0.000182352
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis
[NCBI]
0.00017192
ARSA
[NCBI]
0.000127034
xx male syndrome
[NCBI]
0.000110375
CHS
[NCBI]
0.000107242
DMC
[NCBI]
0.000100472
NCIE1
[NCBI]
9.79464e-05
ISS
[NCBI]
9.79464e-05
ichthyosis vulgaris
[NCBI]
9.36131e-05
metachromatic leukodystrophy due to saposin b deficiency
[NCBI]
9.36131e-05
ARSF
[NCBI]
8.97157e-05
RCDP1
[NCBI]
8.28578e-05
CDPX2
[NCBI]
8.16698e-05
ARSD
[NCBI]
7.94914e-05
mucopolysaccharidosis type iiia
[NCBI]
7.94681e-05
mannosidosis, alpha b, lysosomal
[NCBI]
6.58198e-05
hurler syndrome
[NCBI]
6.47179e-05
mucolipidosis ii
[NCBI]
6.07958e-05
alopecia, androgenetic
[NCBI]
5.49422e-05
ARSB
[NCBI]
4.969e-05
KAL1
[NCBI]
4.72403e-05
ARSC2
[NCBI]
4.48146e-05
dxf68s1e
[NCBI]
4.48146e-05
ARSJ
[NCBI]
3.73924e-05
ARSK
[NCBI]
3.73924e-05
ARSI
[NCBI]
3.73924e-05
ARSG
[NCBI]
3.45916e-05
SULF2
[NCBI]
3.45916e-05
SLOS
[NCBI]
3.36904e-05
SLC25A6
[NCBI]
3.14215e-05
SULF1
[NCBI]
3.14215e-05
PRPS2
[NCBI]
3.03444e-05
GNS
[NCBI]
2.86826e-05
ACO2
[NCBI]
2.68826e-05
NAGA
[NCBI]
2.51581e-05
MAN2B1
[NCBI]
2.33107e-05
OA1
[NCBI]
2.2361e-05
CTCF
[NCBI]
2.03884e-05
SHOX
[NCBI]
2.03884e-05
CF
[NCBI]
1.58088e-05
mucopolysaccharidosis type ii
[NCBI]
1.55031e-05
TTR
[NCBI]
4.52488e-06
RNASE3
[NCBI]
3.83569e-06
VEGF
[NCBI]
3.03338e-06
G6PD
[NCBI]
2.59161e-06
AFP
[NCBI]
4.32999e-07
MPO
[NCBI]
2.99098e-07
CCK
[NCBI]
4.31425e-08
Database Center for Life Science