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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cyanosis [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science