Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hyperventilation	[NCBI]

Gene	Link	Information Gain
GER	[NCBI]	9.91295e-05
TCF4	[NCBI]	7.48011e-05
S100A12	[NCBI]	1.05382e-05
PTH	[NCBI]	8.88997e-06
TCF7L2	[NCBI]	8.88237e-06
DBH	[NCBI]	8.85815e-06
EDN1	[NCBI]	8.26469e-06
MS	[NCBI]	7.68417e-06
VIP	[NCBI]	5.61761e-06
TH	[NCBI]	5.15437e-06
NPY	[NCBI]	4.77554e-06
PRL	[NCBI]	3.90519e-06

OMIM	Link	Information gain
JBTS1	[NCBI]	0.00311482
parkinsonism with alveolar hypoventilation and mental depression	[NCBI]	0.000742146
arima syndrome	[NCBI]	0.000693453
PTHS	[NCBI]	0.000537584
RTT	[NCBI]	9.79408e-05
cutis laxa, autosomal recessive, type i	[NCBI]	7.74297e-05
MLC	[NCBI]	7.3903e-05
TCF4	[NCBI]	7.00104e-05
glycogen storage disease vii	[NCBI]	6.94982e-05
ornithine transcarbamylase deficiency, hyperammonemia due to	[NCBI]	6.02475e-05
HHT	[NCBI]	5.33468e-05
LS	[NCBI]	5.3173e-05
MECP2	[NCBI]	3.87392e-05
XDH	[NCBI]	2.73958e-05
PTH	[NCBI]	2.66308e-05
FMF	[NCBI]	2.33858e-05
NPPA	[NCBI]	2.00967e-05
VIP	[NCBI]	1.93093e-05
TH	[NCBI]	1.65191e-05
NPY	[NCBI]	1.4714e-05
apnea, obstructive sleep	[NCBI]	1.1389e-05
PRL	[NCBI]	9.86858e-06
CF	[NCBI]	2.03751e-12