Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Ketosis	[NCBI]

Gene	Link	Information Gain
OXCT1	[NCBI]	3.25683e-05
SLC2A1	[NCBI]	2.52859e-05
OXCT2	[NCBI]	2.36081e-05
FGF21	[NCBI]	1.36815e-05
AMT	[NCBI]	1.27007e-05
NDUFV1	[NCBI]	1.27007e-05
EBI3	[NCBI]	1.19797e-05
ACAT1	[NCBI]	1.19797e-05
GLDC	[NCBI]	1.18843e-05
PCCB	[NCBI]	1.17939e-05
SLC25A13	[NCBI]	1.03777e-05
IL12A	[NCBI]	9.05023e-06
PPARA	[NCBI]	8.78731e-06
PTPRN	[NCBI]	7.86756e-06
TF	[NCBI]	6.5212e-06
APOB	[NCBI]	5.79164e-06
FASLG	[NCBI]	3.7062e-06
PTH	[NCBI]	2.79151e-06

OMIM	Link	Information gain
IDDM	[NCBI]	0.000674807
GCE	[NCBI]	0.000273254
OXCT1	[NCBI]	0.000243442
succinyl-coa:3-oxoacid coa transferase deficiency	[NCBI]	0.00020285
IVA	[NCBI]	0.000168437
PCCA	[NCBI]	0.000130109
glycogen storage disease 0, liver	[NCBI]	9.48731e-05
glucose transport defect, blood-brain barrier	[NCBI]	7.97839e-05
GPD1	[NCBI]	7.77884e-05
HSS	[NCBI]	7.40678e-05
acyl-coa dehydrogenase, medium-chain, deficiency of	[NCBI]	7.40678e-05
LCAT	[NCBI]	6.96633e-05
MADD	[NCBI]	6.93382e-05
GPD2	[NCBI]	6.9211e-05
myoclonic epilepsy of lafora	[NCBI]	6.88341e-05
pyruvate decarboxylase deficiency	[NCBI]	6.41361e-05
AMT	[NCBI]	5.92612e-05
SLC2A1	[NCBI]	5.37769e-05
transcobalamin ii deficiency	[NCBI]	5.06988e-05
ADCYAP1	[NCBI]	3.3178e-05
TS	[NCBI]	2.48381e-05
TF	[NCBI]	2.30056e-05
APOB	[NCBI]	1.91856e-05
PTH	[NCBI]	3.29613e-06