Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Esophageal Achalasia	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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