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01 Esophageal Achalasia [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.00318304
AAAS [NCBI] 0.000475594
LACRT [NCBI] 1.30838e-05
ACD [NCBI] 1.23044e-05
CASQ1 [NCBI] 1.13646e-05
SOAT2 [NCBI] 1.10365e-05
CALR [NCBI] 9.41997e-06
VIP [NCBI] 9.40882e-06
APTX [NCBI] 8.30638e-06
ATP2A2 [NCBI] 7.44464e-06
PTPN22 [NCBI] 6.16971e-06
NOS1 [NCBI] 5.49791e-06
XRCC1 [NCBI] 5.15073e-06
KRT7 [NCBI] 5.03779e-06
PLN [NCBI] 4.87178e-06
RET [NCBI] 4.32075e-06
CHAT [NCBI] 4.1988e-06
NOS3 [NCBI] 2.91187e-06
NPY [NCBI] 2.73313e-06
NOS2 [NCBI] 2.71113e-06
CDKN1A [NCBI] 1.5393e-06



OMIM


 OMIM Link Information
gain		 01
achalasia, familial esophageal [NCBI] 0.0149491
AAA [NCBI] 0.00211205
deafness, congenital, with vitiligo and achalasia [NCBI] 0.000785962
visceral neuropathy, familial, autosomal dominant [NCBI] 0.000650784
AAAS [NCBI] 0.000604831
achalasia-microcephaly syndrome [NCBI] 0.00026386
leiomyomatosis, esophageal and vulval, with nephropathy [NCBI] 7.73439e-05
SOAT2 [NCBI] 7.71252e-05
SPRY2 [NCBI] 7.19248e-05
MG [NCBI] 5.11125e-05
AMC [NCBI] 4.72104e-05
PHEX [NCBI] 4.57999e-05
RNASE3 [NCBI] 4.29723e-05
VIP [NCBI] 4.09892e-05
KSS [NCBI] 3.46348e-05
SLOS [NCBI] 2.89802e-05
GIST [NCBI] 2.36239e-05
GDNF [NCBI] 1.9395e-05
CHAT [NCBI] 1.75153e-05
NPY [NCBI] 9.48947e-06



Database Center for Life Science