MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Niemann-Pick Diseases
[NCBI]
Gene
Gene
Link
Information
Gain
01
NPC1
[NCBI]
0.00169147
NPC2
[NCBI]
0.000513684
SMPD1
[NCBI]
0.00027845
NPC1L1
[NCBI]
8.90323e-05
RAB9A
[NCBI]
6.09105e-05
PSAP
[NCBI]
4.39952e-05
NR1H3
[NCBI]
3.53009e-05
RAB7A
[NCBI]
3.24807e-05
SREBF1
[NCBI]
2.42991e-05
OSBP
[NCBI]
1.101e-05
ABCA1
[NCBI]
1.03622e-05
CDK5
[NCBI]
9.40063e-06
RAB4A
[NCBI]
9.36102e-06
APOD
[NCBI]
8.86385e-06
VAMP2
[NCBI]
8.70972e-06
RAB8A
[NCBI]
8.53813e-06
CAV1
[NCBI]
8.33073e-06
ABCA2
[NCBI]
7.98524e-06
STARD3
[NCBI]
7.87109e-06
SYP
[NCBI]
7.15964e-06
CHIT1
[NCBI]
7.08849e-06
GDI1
[NCBI]
6.83043e-06
ABCG1
[NCBI]
6.03416e-06
ABCG8
[NCBI]
5.99725e-06
LY96
[NCBI]
5.99725e-06
SCP2
[NCBI]
5.92577e-06
LAMP2
[NCBI]
5.89114e-06
NAGA
[NCBI]
5.63721e-06
CCL18
[NCBI]
5.55113e-06
SREBF2
[NCBI]
5.39125e-06
BECN1
[NCBI]
5.29262e-06
NEFM
[NCBI]
5.13298e-06
CTSD
[NCBI]
5.13298e-06
CASP6
[NCBI]
4.87211e-06
GFAP
[NCBI]
4.67615e-06
GBA
[NCBI]
4.37922e-06
LCAT
[NCBI]
4.21009e-06
CD1D
[NCBI]
4.12589e-06
APOA1
[NCBI]
3.57667e-06
NEFH
[NCBI]
3.07295e-06
TERT
[NCBI]
2.6157e-06
SNCA
[NCBI]
1.2558e-06
CASP3
[NCBI]
1.19907e-06
CCK
[NCBI]
1.0281e-06
BDNF
[NCBI]
8.98223e-07
TNFSF10
[NCBI]
7.5496e-07
NOS3
[NCBI]
7.15124e-07
NPY
[NCBI]
5.91442e-07
NOS2
[NCBI]
5.767e-07
TNF
[NCBI]
5.59045e-07
BAX
[NCBI]
3.02499e-07
AFP
[NCBI]
2.11362e-07
APOE
[NCBI]
1.07544e-07
OMIM
OMIM
Link
Information
gain
01
NPC1
[NCBI]
0.00675885
niemann-pick disease, type a
[NCBI]
0.0023399
NPC1
[NCBI]
0.00206265
niemann-pick disease, type b
[NCBI]
0.00198371
SMPD1
[NCBI]
0.00165303
NPC2
[NCBI]
0.000493502
niemann-pick disease, type c2
[NCBI]
0.000473056
gm1-gangliosidosis, type i
[NCBI]
0.000161757
NPC1L1
[NCBI]
0.000148931
sea-blue histiocyte disease
[NCBI]
0.000131569
PSAP
[NCBI]
0.000120264
CF
[NCBI]
8.68072e-05
ceroid storage disease
[NCBI]
7.69809e-05
B4GALNT1
[NCBI]
7.44041e-05
APOD
[NCBI]
7.34931e-05
bile acid synthesis defect, congenital, 4
[NCBI]
6.74182e-05
alzheimer disease, susceptibility to, mitochondrial
[NCBI]
5.71674e-05
metachromatic leukodystrophy due to saposin b deficiency
[NCBI]
5.37803e-05
CDK5
[NCBI]
5.10581e-05
LAMP1
[NCBI]
4.95545e-05
ABCA2
[NCBI]
4.95545e-05
JUN
[NCBI]
4.448e-05
MTCO2
[NCBI]
3.86652e-05
MTCO1
[NCBI]
3.55598e-05
fucosidosis
[NCBI]
3.03405e-05
wolman disease
[NCBI]
2.71983e-05
AMACR
[NCBI]
2.61445e-05
metachromatic leukodystrophy
[NCBI]
2.3146e-05
NR1I2
[NCBI]
2.31067e-05
krabbe disease
[NCBI]
1.6278e-05
PDCD8
[NCBI]
1.58885e-05
TNF
[NCBI]
1.55515e-05
TSD
[NCBI]
1.04081e-05
GFAP
[NCBI]
9.23651e-06
AD
[NCBI]
3.60762e-06
thrombocytopenic purpura, autoimmune
[NCBI]
1.95319e-06
CCK
[NCBI]
1.01322e-06
BDNF
[NCBI]
8.40145e-07
AFP
[NCBI]
4.23217e-07
NPY
[NCBI]
7.68691e-08
Database Center for Life Science