Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Hirschsprung Disease [NCBI]


Gene


Gene Link Information
Gain
01
RET [NCBI] 0.00102467
HSCRM1 [NCBI] 0.000733332
HSCRM2 [NCBI] 0.000401057
HSCRS3 [NCBI] 0.000401057
HSCRS2 [NCBI] 0.000401057
SOX10 [NCBI] 0.000327923
GDNF [NCBI] 0.000288818
ACHE [NCBI] 0.000287488
EDNRB [NCBI] 0.000276294
ZEB2 [NCBI] 0.000270148
EDN3 [NCBI] 0.000267292
PHOX2B [NCBI] 0.000182419
VIP [NCBI] 6.26756e-05
NRTN [NCBI] 3.66422e-05
GFRA2 [NCBI] 3.0227e-05
L1CAM [NCBI] 2.82275e-05
SHC1 [NCBI] 2.66106e-05
GFRA1 [NCBI] 2.64663e-05
KIAA1279 [NCBI] 2.34233e-05
MNX1 [NCBI] 2.31553e-05
RASGEF1A [NCBI] 2.1942e-05
NPY [NCBI] 2.18186e-05
GFRA3 [NCBI] 2.01464e-05
GFRA4 [NCBI] 1.95139e-05
PAX3 [NCBI] 1.87999e-05
KCNN3 [NCBI] 1.48963e-05
PYY [NCBI] 1.32075e-05
GRP [NCBI] 1.21553e-05
TLX1 [NCBI] 1.1744e-05
NKX2-1 [NCBI] 1.04959e-05
KCNN2 [NCBI] 1.00708e-05
PSPN [NCBI] 9.48803e-06
BCHE [NCBI] 8.94765e-06
NGFR [NCBI] 8.70586e-06
TH [NCBI] 7.98974e-06
SOX11 [NCBI] 7.77263e-06
CTNNAL1 [NCBI] 7.77263e-06
ARTN [NCBI] 7.60134e-06
HOXA4 [NCBI] 7.60134e-06
POU3F1 [NCBI] 7.44574e-06
HOXD9 [NCBI] 7.44574e-06
FRS2 [NCBI] 6.93582e-06
ECE1 [NCBI] 6.54438e-06
GRB10 [NCBI] 6.45921e-06
LAMA2 [NCBI] 6.37813e-06
NTRK3 [NCBI] 6.30077e-06
GAL [NCBI] 6.22681e-06
IHH [NCBI] 6.22681e-06
LAMA5 [NCBI] 6.08798e-06
HOXB7 [NCBI] 6.02264e-06
TLX3 [NCBI] 5.7841e-06
STX1A [NCBI] 5.7841e-06
HOXA13 [NCBI] 5.57536e-06
PLCG1 [NCBI] 5.52701e-06
SIP1 [NCBI] 5.38986e-06
DHCR7 [NCBI] 5.03561e-06
CDX1 [NCBI] 4.89965e-06
GFAP [NCBI] 4.80961e-06
PLEK [NCBI] 4.71474e-06
ITGB2 [NCBI] 4.47152e-06
LAMA1 [NCBI] 4.35064e-06
NEFM [NCBI] 4.2166e-06
HOXA9 [NCBI] 3.83681e-06
NID1 [NCBI] 3.63127e-06
ESD [NCBI] 3.60191e-06
ADCYAP1 [NCBI] 3.26364e-06
SOX9 [NCBI] 3.20635e-06
CD22 [NCBI] 2.68891e-06
MITF [NCBI] 2.6498e-06
GRB2 [NCBI] 2.49631e-06
FGF7 [NCBI] 2.47568e-06
KIT [NCBI] 2.37687e-06
XRCC5 [NCBI] 1.90428e-06
CHGA [NCBI] 1.81812e-06
EGR1 [NCBI] 1.76914e-06
MUC2 [NCBI] 1.69537e-06
MEN1 [NCBI] 1.64375e-06
SLC2A1 [NCBI] 1.48218e-06
CHAT [NCBI] 1.0043e-06
LIF [NCBI] 9.43178e-07
NGF [NCBI] 7.15657e-07
HRAS [NCBI] 3.6142e-07
BDNF [NCBI] 3.23604e-07




OMIM


OMIM Link Information
gain
01
HSCR1 [NCBI] 0.0116958
HSCR9 [NCBI] 0.00342502
RET [NCBI] 0.00239718
mowat-wilson syndrome [NCBI] 0.00134837
EDNRB [NCBI] 0.00118643
waardenburg-shah syndrome [NCBI] 0.00113449
HSCR7 [NCBI] 0.00111789
HSCR6 [NCBI] 0.00111789
HSCR5 [NCBI] 0.00111789
HSCR8 [NCBI] 0.00111789
HSCR2 [NCBI] 0.00111266
ACHE [NCBI] 0.00110358
EDN3 [NCBI] 0.000941279
GDNF [NCBI] 0.000753583
SOX10 [NCBI] 0.000739638
ZEB2 [NCBI] 0.000627761
visceral neuropathy, familial, autosomal recessive [NCBI] 0.000625244
goldberg-shprintzen megacolon syndrome [NCBI] 0.000554724
autonomic control, congenital failure of [NCBI] 0.000430059
SRS [NCBI] 0.000217145
VIP [NCBI] 0.000197943
neuronal intestinal dysplasia, type b [NCBI] 0.000169137
abcd syndrome [NCBI] 0.000169137
PHOX2B [NCBI] 0.00016206
PCWH [NCBI] 0.000155181
L1CAM [NCBI] 0.000132431
WS2A [NCBI] 0.000107388
GFRA1 [NCBI] 0.000101898
hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [NCBI] 9.99857e-05
hirschsprung disease with polydactyly, renal agenesis, and deafness [NCBI] 9.99857e-05
hirschsprung disease with hypoplastic nails and dysmorphic facial features [NCBI] 9.99857e-05
brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia [NCBI] 9.99857e-05
hirschsprung disease with type d brachydactyly [NCBI] 9.99857e-05
WS2E [NCBI] 9.99857e-05
SLOS [NCBI] 8.33253e-05
NKX2-1 [NCBI] 7.10697e-05
corpus callosum, partial agenesis of, x-linked [NCBI] 6.90987e-05
GFRA3 [NCBI] 6.46921e-05
FRS2 [NCBI] 6.46921e-05
KIAA1279 [NCBI] 6.46921e-05
CHH [NCBI] 5.4272e-05
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked [NCBI] 5.13618e-05
GFRA2 [NCBI] 5.09261e-05
protoporphyria, erythropoietic [NCBI] 4.58974e-05
NRTN [NCBI] 4.57395e-05
PYY [NCBI] 4.25372e-05
NPY [NCBI] 4.25298e-05
currarino syndrome [NCBI] 4.20286e-05
NGFR [NCBI] 3.83345e-05
G22P1 [NCBI] 3.78927e-05
BBS [NCBI] 3.73093e-05
ECE1 [NCBI] 3.48328e-05
AFD1 [NCBI] 3.40507e-05
BCHE [NCBI] 3.11557e-05
OPTB1 [NCBI] 3.09669e-05
MKKS [NCBI] 2.93901e-05
ADCYAP1 [NCBI] 2.81841e-05
SPG3A [NCBI] 2.55035e-05
CES [NCBI] 2.16102e-05
neuroblastoma [NCBI] 2.13323e-05
ERBB2 [NCBI] 2.03331e-05
ITGB2 [NCBI] 1.9271e-05
RSTS [NCBI] 1.90728e-05
ESD [NCBI] 1.90242e-05
ALGS1 [NCBI] 1.73619e-05
PAX3 [NCBI] 1.48568e-05
ASS [NCBI] 1.36115e-05
GAL [NCBI] 9.46081e-06
TH [NCBI] 8.67584e-06
HPS [NCBI] 7.36936e-06
CHS [NCBI] 4.63646e-06
NGFB [NCBI] 3.56822e-06
BDNF [NCBI] 1.72213e-06
APC [NCBI] 9.64356e-07
GFAP [NCBI] 8.20814e-07
CHAT [NCBI] 1.57194e-08




Database Center for Life Science