Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Megacolon [NCBI]

Gene


 Gene Link Information
Gain		 01
HSCRM1 [NCBI] 0.000415947
ACHE [NCBI] 3.01881e-05
TLX2 [NCBI] 1.43136e-05
HOXA4 [NCBI] 1.32017e-05
NRTN [NCBI] 1.22289e-05
CHRM2 [NCBI] 1.16119e-05
EDN3 [NCBI] 1.1487e-05
CDX1 [NCBI] 1.04715e-05
ZEB2 [NCBI] 1.03743e-05
SOX10 [NCBI] 9.81521e-06
HOXA9 [NCBI] 9.37668e-06
TIA1 [NCBI] 8.79993e-06
VIP [NCBI] 5.48734e-06
CCK [NCBI] 5.27401e-06



OMIM


 OMIM Link Information
gain		 01
deafness, congenital, with vitiligo and achalasia [NCBI] 0.00107364
MGS [NCBI] 0.00107364
tibia, hypoplasia of, with polydactyly [NCBI] 0.00078076
HSCR1 [NCBI] 0.000775467
WS1 [NCBI] 0.00029386
waardenburg-shah syndrome [NCBI] 0.000267291
TLX2 [NCBI] 0.000188652
PBT [NCBI] 0.000174706
autonomic control, congenital failure of [NCBI] 0.000143986
aganglionosis, total intestinal [NCBI] 0.000132242
harrod syndrome [NCBI] 0.000132242
hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect [NCBI] 0.000132242
CHH [NCBI] 0.00011729
EDNRB [NCBI] 0.000115628
ACHE [NCBI] 0.000112731
goldberg-shprintzen megacolon syndrome [NCBI] 8.57315e-05
mowat-wilson syndrome [NCBI] 7.27487e-05
ZEB2 [NCBI] 5.73625e-05
EDN3 [NCBI] 5.44203e-05
SOX10 [NCBI] 5.21546e-05
SDS [NCBI] 4.3407e-05
VIP [NCBI] 1.64974e-05
CCK [NCBI] 1.52448e-05
CF [NCBI] 9.25612e-08



Database Center for Life Science