Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Cyanosis	[NCBI]

Gene	Link	Information Gain
GER	[NCBI]	0.000317425
HBG2	[NCBI]	3.65155e-05
HIF1A	[NCBI]	1.11487e-05
HGF	[NCBI]	1.10971e-05
VEGFA	[NCBI]	9.74869e-06
CBX4	[NCBI]	9.6957e-06
THBD	[NCBI]	9.62424e-06
PHOX2B	[NCBI]	9.12226e-06
GHRL	[NCBI]	7.78942e-06
HBB	[NCBI]	7.55857e-06
PF4	[NCBI]	6.86956e-06
TNF	[NCBI]	5.7345e-06
IL6	[NCBI]	4.73064e-06
NOS3	[NCBI]	4.60392e-06
PTEN	[NCBI]	4.52119e-06
NOS2	[NCBI]	4.39235e-06

OMIM	Link	Information gain
DIP	[NCBI]	0.00111789
HBB	[NCBI]	0.000431173
breath-holding spells	[NCBI]	0.000334902
HBG2	[NCBI]	0.000308939
methemoglobinemia due to deficiency of methemoglobin reductase	[NCBI]	0.000254231
autonomic control, congenital failure of	[NCBI]	0.000152857
pulmonary nodular lymphoid hyperplasia, familial	[NCBI]	0.000136591
cyanosis and hepatic disease	[NCBI]	0.000136591
venular insufficiency, systemic	[NCBI]	0.000136591
rombo syndrome	[NCBI]	0.000114122
laryngeal abductor paralysis	[NCBI]	0.000114122
encephalopathy, ethylmalonic	[NCBI]	9.27854e-05
ebstein anomaly	[NCBI]	9.00744e-05
corpus callosum, agenesis of	[NCBI]	8.5726e-05
LDS	[NCBI]	7.9483e-05
asplenia with cardiovascular anomalies	[NCBI]	7.2296e-05
GACI	[NCBI]	6.99862e-05
pulmonary fibrosis, idiopathic	[NCBI]	6.61745e-05
HBA1	[NCBI]	6.3163e-05
charge syndrome	[NCBI]	6.17565e-05
CMTC	[NCBI]	5.86494e-05
TLX3	[NCBI]	5.80874e-05
HSAN3	[NCBI]	5.7959e-05
VEGF	[NCBI]	4.56092e-05
TGFBR2	[NCBI]	4.08732e-05
HGF	[NCBI]	1.78182e-05
PF4	[NCBI]	1.55531e-05
TNF	[NCBI]	1.54248e-06