Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Acyl-CoA Dehydrogenase, Long-Chain	[NCBI]

Gene	Link	Information Gain
ACADVL	[NCBI]	6.50194e-05
ACADL	[NCBI]	2.92408e-05
ACAD9	[NCBI]	1.36355e-05
HADHA	[NCBI]	6.53898e-06
UCP3	[NCBI]	4.16182e-06
ACADM	[NCBI]	3.92276e-06
DLG4	[NCBI]	3.30059e-06
GPSN2	[NCBI]	2.31943e-06
CPT1C	[NCBI]	2.28108e-06
HSD17B12	[NCBI]	2.21776e-06
ETFB	[NCBI]	2.12369e-06
ETFA	[NCBI]	2.10456e-06
ACAD8	[NCBI]	2.10456e-06
SC5DL	[NCBI]	2.05424e-06
HADHB	[NCBI]	2.0119e-06
IVD	[NCBI]	2.0119e-06
ACADS	[NCBI]	1.987e-06
CPT1A	[NCBI]	1.89698e-06
NR2F1	[NCBI]	1.55659e-06
PC	[NCBI]	1.51085e-06
UCP1	[NCBI]	1.43325e-06
CS	[NCBI]	1.23125e-06

OMIM	Link	Information gain
acyl-coa dehydrogenase, very long-chain, deficiency of	[NCBI]	0.00334516
ACADVL	[NCBI]	0.000844718
acyl-coa dehydrogenase, long-chain, deficiency of	[NCBI]	0.000595192
ACADM	[NCBI]	0.000482545
acyl-coa dehydrogenase, medium-chain, deficiency of	[NCBI]	0.000429613
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency	[NCBI]	0.000315171
MADD	[NCBI]	0.000291846
ACAD9	[NCBI]	0.000182001
ACADL	[NCBI]	0.000182001
acyl-coa dehydrogenase family, member 9, deficiency of	[NCBI]	0.000174818
IVD	[NCBI]	0.000118946
ACADS	[NCBI]	0.000109271
sudden infant death syndrome	[NCBI]	9.64951e-05
acyl-coa dehydrogenase, short-chain, deficiency of	[NCBI]	8.57298e-05
adrenoleukodystrophy, autosomal neonatal form	[NCBI]	6.70245e-05
HSD17B12	[NCBI]	4.53551e-05
GPSN2	[NCBI]	3.79327e-05
ETFDH	[NCBI]	2.99888e-05
HADHB	[NCBI]	2.92223e-05
ALD	[NCBI]	2.63716e-05
DLG4	[NCBI]	2.46929e-05
ADRP	[NCBI]	2.04936e-05
PC	[NCBI]	1.43889e-05
PPARA	[NCBI]	1.43489e-05
UCP1	[NCBI]	1.34575e-05