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01 Comorbidity [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
MDD [NCBI] 0.0110259
apnea, obstructive sleep [NCBI] 0.00348761
GTS [NCBI] 0.00114123
ANON1 [NCBI] 0.00103726
BULN1 [NCBI] 0.00094328
HDLCQ1 [NCBI] 0.000943148
asthma-related traits, susceptibility to, 4 [NCBI] 0.000943148
panic disorder 2 [NCBI] 0.000943148
ETL4 [NCBI] 0.000943148
SCA20 [NCBI] 0.000679307
testicular germ cell tumor 1 [NCBI] 0.000679307
speech-sound disorder [NCBI] 0.000516945
MAFD1 [NCBI] 0.000483273
ETM2 [NCBI] 0.000469981
EKD1 [NCBI] 0.000405661
CF [NCBI] 0.000353274
centralopathic epilepsy [NCBI] 0.000333604
AD [NCBI] 0.000323172
ETL2 [NCBI] 0.000299778
IBGC1 [NCBI] 0.000285194
autism [NCBI] 0.000280797
PAND1 [NCBI] 0.000259541
abdominal obesity-metabolic syndrome [NCBI] 0.000227686
VRNI [NCBI] 0.000213695
ADHD [NCBI] 0.000196989
restless legs syndrome, susceptibility to, 1 [NCBI] 0.000166678
PD [NCBI] 0.000156675
CD [NCBI] 0.000152399
OCD1 [NCBI] 0.000148025
GEPD [NCBI] 0.000145599
kabuki syndrome [NCBI] 0.000129931
behcet syndrome [NCBI] 0.000117181
APOE [NCBI] 0.000116358
klippel-trenaunay-weber syndrome [NCBI] 9.88807e-05
APC [NCBI] 9.63223e-05
iron overload in africa [NCBI] 8.95769e-05
SCZD [NCBI] 8.02531e-05
CADASIL [NCBI] 7.69753e-05
RP [NCBI] 7.14624e-05
CJD [NCBI] 7.02442e-05
aortic aneurysm, familial thoracic 3 [NCBI] 6.42436e-05
HSA [NCBI] 6.42436e-05
brain small vessel disease with hemorrhage [NCBI] 6.42436e-05
EPO [NCBI] 6.20535e-05
KLK3 [NCBI] 6.19893e-05
FA [NCBI] 6.10405e-05
EIG [NCBI] 5.80695e-05
stroke, ischemic [NCBI] 5.70921e-05
JPHT [NCBI] 5.39663e-05
brugada syndrome 2 [NCBI] 5.39663e-05
SHBG [NCBI] 5.1996e-05
alcohol dependence [NCBI] 5.02532e-05
MBL2 [NCBI] 4.81468e-05
pelizaeus-merzbacher-like disease, autosomal recessive, 1 [NCBI] 4.73644e-05
cardiomyopathy, dilated, autosomal recessive [NCBI] 4.73644e-05
TINU [NCBI] 4.25081e-05
alopecia, androgenetic [NCBI] 4.0492e-05
amyloidosis vi [NCBI] 3.61692e-05
CRC [NCBI] 3.61438e-05
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 3.55309e-05
IS1 [NCBI] 3.46417e-05
PTH [NCBI] 3.28885e-05
HS1BP3 [NCBI] 3.25817e-05
MTHFR [NCBI] 3.18408e-05
CNTNAP2 [NCBI] 3.05638e-05
PRKCH [NCBI] 3.05638e-05
GPD1L [NCBI] 3.05638e-05
hypoalphalipoproteinemia, primary [NCBI] 3.05598e-05
aspirin resistance [NCBI] 3.05598e-05
PLXNA2 [NCBI] 2.90642e-05
CPB2 [NCBI] 2.89382e-05
HCHWAD [NCBI] 2.8535e-05
GJC2 [NCBI] 2.787e-05
TS [NCBI] 2.61022e-05
CYP4A11 [NCBI] 2.60283e-05
SCN1B [NCBI] 2.46276e-05
HTR1B [NCBI] 2.40354e-05
HOXA1 [NCBI] 2.40354e-05
ACCPN [NCBI] 2.36504e-05
ZNF9 [NCBI] 2.34974e-05
OLIG2 [NCBI] 2.30048e-05
polycystic kidneys [NCBI] 2.23359e-05
TNNI3 [NCBI] 2.21287e-05
HMS1 [NCBI] 2.10872e-05
SCZD4 [NCBI] 2.10872e-05
MAFD6 [NCBI] 2.00697e-05
G6PD [NCBI] 1.99719e-05
DRD3 [NCBI] 1.98103e-05
APTX [NCBI] 1.92884e-05
DYT1 [NCBI] 1.8159e-05
velocardiofacial syndrome [NCBI] 1.80936e-05
EAOH [NCBI] 1.7936e-05
LAM [NCBI] 1.78948e-05
CVID [NCBI] 1.77398e-05
TGFBR2 [NCBI] 1.75746e-05
SMAD4 [NCBI] 1.73923e-05
brugada syndrome 1 [NCBI] 1.70283e-05
SLC6A4 [NCBI] 1.62994e-05
SCA10 [NCBI] 1.61792e-05
ADIPOQ [NCBI] 1.55668e-05
APOB [NCBI] 1.55028e-05
ETM1 [NCBI] 1.5383e-05
RA [NCBI] 1.50447e-05
CSF3 [NCBI] 1.45041e-05
MLC [NCBI] 1.39294e-05
UGT1A1 [NCBI] 1.33442e-05
CRMO [NCBI] 1.32639e-05
TG [NCBI] 1.32128e-05
protein c deficiency, congenital thrombotic disease due to [NCBI] 1.30063e-05
NR0B2 [NCBI] 1.26114e-05
CRH [NCBI] 1.20985e-05
LCA1 [NCBI] 1.20391e-05
BDNF [NCBI] 1.18641e-05
ASS [NCBI] 1.17671e-05
RTT [NCBI] 1.15374e-05
lymphoma, non-hodgkin, familial [NCBI] 1.14374e-05
ALB [NCBI] 1.12963e-05
PG [NCBI] 1.0449e-05
VEGF [NCBI] 9.98694e-06
homocysteinemia [NCBI] 9.94309e-06
CCND1 [NCBI] 9.60983e-06
FPLD2 [NCBI] 9.48106e-06
MFS [NCBI] 9.25569e-06
DBI [NCBI] 8.85338e-06
UCP1 [NCBI] 8.85338e-06
AGER [NCBI] 8.74383e-06
IL6 [NCBI] 8.39546e-06
thrombocytopenic purpura, autoimmune [NCBI] 8.28756e-06
drug metabolism, poor, cyp2d6-related [NCBI] 7.83561e-06
DNMT1 [NCBI] 7.76632e-06
COMP [NCBI] 6.88384e-06
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity [NCBI] 6.78277e-06
BL [NCBI] 6.69377e-06
LKS [NCBI] 6.15359e-06
SMEI [NCBI] 6.15359e-06
GDNF [NCBI] 6.01176e-06
NF1 [NCBI] 5.66179e-06
TSD [NCBI] 5.36081e-06
LPL [NCBI] 5.33444e-06
JPS [NCBI] 5.30474e-06
DM2 [NCBI] 5.04472e-06
ALGS1 [NCBI] 4.7953e-06
LRP1 [NCBI] 4.71981e-06
leber optic atrophy [NCBI] 4.58838e-06
PMCH [NCBI] 4.57827e-06
LDLR [NCBI] 4.56441e-06
TPO [NCBI] 4.27196e-06
obesity [NCBI] 3.8946e-06
down syndrome [NCBI] 3.8946e-06
ARPKD [NCBI] 3.31003e-06
PRL [NCBI] 3.14805e-06
ACE [NCBI] 3.07043e-06
PWS [NCBI] 2.92578e-06
SLE [NCBI] 2.60692e-06
BWS [NCBI] 2.60299e-06
TLR4 [NCBI] 2.49555e-06
MUC1 [NCBI] 2.33515e-06
FTD [NCBI] 2.2917e-06
AVP [NCBI] 2.2897e-06
SOD2 [NCBI] 2.24233e-06
TFPI [NCBI] 2.1655e-06
HD [NCBI] 1.9094e-06
TNF [NCBI] 1.86567e-06
CHH [NCBI] 1.81455e-06
COMT [NCBI] 1.68038e-06
PXE [NCBI] 1.5455e-06
AS [NCBI] 1.43351e-06
POMC [NCBI] 1.29088e-06
TNFRSF11B [NCBI] 1.1887e-06
hypertension, essential [NCBI] 1.18555e-06
AVSD [NCBI] 1.18555e-06
PMD [NCBI] 1.12585e-06
HPS [NCBI] 9.10509e-07
HSCR1 [NCBI] 8.59621e-07
MG [NCBI] 6.20248e-07
AFP [NCBI] 3.93945e-07
BBS [NCBI] 3.49648e-07
MODY [NCBI] 2.10556e-07
MS [NCBI] 1.7209e-07
FMF [NCBI] 1.68191e-07
temporal arteritis [NCBI] 1.34184e-07
NPY [NCBI] 1.29775e-07
CEACAM5 [NCBI] 7.48904e-08
ACHE [NCBI] 5.90455e-08
DBA [NCBI] 5.33099e-10



Database Center for Life Science