MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Acetyl-CoA C-Acyltransferase
[NCBI]
Gene
Gene
Link
Information
Gain
01
ZWS1
[NCBI]
0.000299491
ACAT1
[NCBI]
1.94994e-05
ACAA1
[NCBI]
1.62224e-05
SCP2
[NCBI]
1.53881e-05
HADHB
[NCBI]
7.12804e-06
HADHA
[NCBI]
6.69319e-06
HSD17B4
[NCBI]
6.10729e-06
ACAA2
[NCBI]
5.00637e-06
KAT2A
[NCBI]
3.91805e-06
DECR1
[NCBI]
2.08968e-06
PEX7
[NCBI]
2.06221e-06
PEX14
[NCBI]
1.91531e-06
PEX1
[NCBI]
1.81579e-06
ABCD3
[NCBI]
1.75977e-06
OTC
[NCBI]
1.67712e-06
OXCT2
[NCBI]
1.63436e-06
BNIP3
[NCBI]
1.59982e-06
KAT2B
[NCBI]
1.53265e-06
PLTP
[NCBI]
1.38979e-06
EP300
[NCBI]
1.28995e-06
MYOD1
[NCBI]
1.28635e-06
CS
[NCBI]
1.2814e-06
ITPR1
[NCBI]
1.18391e-06
NR1H3
[NCBI]
1.08698e-06
CREBBP
[NCBI]
1.07674e-06
CAT
[NCBI]
7.99754e-07
VIP
[NCBI]
6.95494e-07
APOE
[NCBI]
6.86908e-07
OMIM
OMIM
Link
Information
gain
01
medium chain 3-ketoacyl-coa thiolase deficiency
[NCBI]
0.003491
alpha-methylacetoacetic aciduria
[NCBI]
0.00144526
d-bifunctional protein deficiency
[NCBI]
0.000364074
hydroxyacyl-coa dehydrogenase ii deficiency
[NCBI]
0.000271966
RCDP1
[NCBI]
0.000221788
ACAT1
[NCBI]
0.000195963
SCP2
[NCBI]
0.000160067
ZS
[NCBI]
0.00014554
trifunctional protein deficiency
[NCBI]
0.000101113
PEX7
[NCBI]
9.99605e-05
ALD
[NCBI]
9.81696e-05
ACAA1
[NCBI]
8.80061e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
[NCBI]
8.67029e-05
adrenoleukodystrophy, autosomal neonatal form
[NCBI]
7.51836e-05
HADHB
[NCBI]
7.41441e-05
HSD17B4
[NCBI]
6.28755e-05
ACAA2
[NCBI]
4.15969e-05
ACADM
[NCBI]
3.93077e-05
SOAT1
[NCBI]
2.93539e-05
OTC
[NCBI]
2.18177e-05
PPARA
[NCBI]
2.12003e-05
PLTP
[NCBI]
1.48221e-05
CAT
[NCBI]
3.60463e-06
CF
[NCBI]
3.3039e-06
APOE
[NCBI]
3.09275e-06
VIP
[NCBI]
1.9688e-06
Database Center for Life Science