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01 3-Hydroxyacyl CoA Dehydrogenases [NCBI]

Gene


 Gene Link Information
Gain		 01
LOC390586 [NCBI] 0.000299491
CS [NCBI] 0.000153382
HSD17B10 [NCBI] 0.000133707
HSD17B4 [NCBI] 7.66858e-05
HADHA [NCBI] 3.69096e-05
HADH [NCBI] 2.9429e-05
OXCT2 [NCBI] 1.01206e-05
EHHADH [NCBI] 9.32818e-06
HADHB [NCBI] 8.07615e-06
SCP2 [NCBI] 6.6992e-06
UCP3 [NCBI] 5.68039e-06
APP [NCBI] 5.46992e-06
CRYL1 [NCBI] 4.38169e-06
FABP7 [NCBI] 3.09961e-06
HSD11B1L [NCBI] 2.33023e-06
PPARGC1A [NCBI] 2.25838e-06
SREBF1 [NCBI] 1.90253e-06
ACAD9 [NCBI] 1.83145e-06
ACADL [NCBI] 1.758e-06
ACAA1 [NCBI] 1.71829e-06
NDUFS1 [NCBI] 1.68373e-06
DECR1 [NCBI] 1.65313e-06
MDH2 [NCBI] 1.57803e-06
SLC27A4 [NCBI] 1.57803e-06
SLC16A7 [NCBI] 1.57803e-06
HUWE1 [NCBI] 1.54715e-06
PEX13 [NCBI] 1.52839e-06
PEX14 [NCBI] 1.47891e-06
PEX5 [NCBI] 1.44371e-06
NR1D1 [NCBI] 1.33655e-06
ABCD3 [NCBI] 1.32363e-06
RBP1 [NCBI] 1.26368e-06
NRF1 [NCBI] 1.22913e-06
FABP3 [NCBI] 1.17835e-06
NR2F1 [NCBI] 1.17115e-06
TFAM [NCBI] 1.15731e-06
SERPINA3 [NCBI] 1.1296e-06
TXN [NCBI] 1.0937e-06
CD36 [NCBI] 1.0937e-06
ABCD1 [NCBI] 1.06368e-06
UCP1 [NCBI] 1.04836e-06
ITPR1 [NCBI] 7.52076e-07
MB [NCBI] 7.45487e-07
IBSP [NCBI] 7.31475e-07
SLC2A4 [NCBI] 6.97368e-07
CD68 [NCBI] 4.7652e-07
IL6 [NCBI] 4.58113e-07
PTEN [NCBI] 4.55538e-07
LPL [NCBI] 3.7107e-07
CCK [NCBI] 2.70538e-07
CDKN1A [NCBI] 2.12209e-07
NPY [NCBI] 2.07033e-07
CASP3 [NCBI] 1.82802e-07



OMIM


 OMIM Link Information
gain		 01
opticocochleodentate degeneration [NCBI] 0.003491
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 0.00318887
d-bifunctional protein deficiency [NCBI] 0.00167487
trifunctional protein deficiency [NCBI] 0.000913934
3-@hydroxyacyl-coa dehydrogenase deficiency [NCBI] 0.00064588
HADH [NCBI] 0.000456883
HADHA [NCBI] 0.000454713
HSD17B10 [NCBI] 0.000424179
HSD17B4 [NCBI] 0.000364317
HHF4 [NCBI] 0.000258936
acyl-coa dehydrogenase, long-chain, deficiency of [NCBI] 0.000226742
MRXS10 [NCBI] 0.000160829
BRRS [NCBI] 0.000145446
adrenoleukodystrophy, autosomal neonatal form [NCBI] 0.000138533
HHF2 [NCBI] 0.000132561
PPARA [NCBI] 0.000122426
hydroxyacyl-coa dehydrogenase ii deficiency [NCBI] 9.55255e-05
peroxisomal acyl-coa oxidase deficiency [NCBI] 9.22784e-05
EHHADH [NCBI] 8.78206e-05
sudden infant death syndrome [NCBI] 8.26058e-05
ACADM [NCBI] 7.31116e-05
HADHB [NCBI] 6.37392e-05
MADD [NCBI] 5.73797e-05
ALD [NCBI] 5.63332e-05
GAL [NCBI] 5.26001e-05
CDSP [NCBI] 4.92124e-05
SLS [NCBI] 4.75856e-05
UCP3 [NCBI] 3.63544e-05
ZS [NCBI] 3.55627e-05
ACAA1 [NCBI] 3.36516e-05
ACAD9 [NCBI] 3.18335e-05
PEX13 [NCBI] 2.70741e-05
FOXA2 [NCBI] 2.38652e-05
PEX7 [NCBI] 2.18793e-05
ACOX1 [NCBI] 2.0812e-05
SLC25A20 [NCBI] 2.06221e-05
DLD [NCBI] 2.06221e-05
ALDH3A2 [NCBI] 1.94562e-05
UCP1 [NCBI] 1.20288e-05
SLC2A4 [NCBI] 1.14348e-05
APP [NCBI] 1.06607e-05
MB [NCBI] 5.62689e-06
LPL [NCBI] 4.40331e-07
NPY [NCBI] 3.38709e-07
CCK [NCBI] 5.74805e-09



Database Center for Life Science