Gendoo

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