Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Acetyl-CoA C-Acyltransferase	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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