Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6439
Gene Symbol: SFTPB
SFTPB
0.510 Biomarker disease RGD Respiratory distress after intratracheal bleomycin: selective deficiency of surfactant proteins B and C. 11504697 2001
Entrez Id: 6439
Gene Symbol: SFTPB
SFTPB
0.510 SusceptibilityMutation disease ORPHANET Surfactant proteins A and B as interactive genetic determinants of neonatal respiratory distress syndrome. 11063734 2000
Entrez Id: 6439
Gene Symbol: SFTPB
SFTPB
0.510 Biomarker disease BEFREE Previous deaths were mistakenly attributed to hyaline membrane disease (HMD), congenital Mycoplasma hominis infection, and pulmonary hypertension, however, following the diagnosis in the proposita, SP-B deficiency was also confirmed in her deceased siblings by immunohistochemical staining of autopsy specimens. 11041444 2000
Entrez Id: 6440
Gene Symbol: SFTPC
SFTPC
0.500 Biomarker disease RGD Respiratory distress after intratracheal bleomycin: selective deficiency of surfactant proteins B and C. 11504697 2001
Entrez Id: 6440
Gene Symbol: SFTPC
SFTPC
0.500 SusceptibilityMutation disease ORPHANET
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.300 GeneticVariation disease ORPHANET Lung disease caused by ABCA3 mutations. 27516224 2017
Entrez Id: 3383
Gene Symbol: ICAM1
ICAM1
0.200 Biomarker disease RGD Pre-treatment with glutamine attenuates lung injury in rats subjected to intestinal ischaemia-reperfusion. 19837405 2011
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.200 Biomarker disease MGD VEGF signalling controls GnRH neuron survival via NRP1 independently of KDR and blood vessels. 21828096 2011
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.200 Biomarker disease MGD Vascular endothelial growth factor controls neuronal migration and cooperates with Sema3A to pattern distinct compartments of the facial nerve. 15545635 2004
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.200 Biomarker disease MGD VEGF: a modifier of the del22q11 (DiGeorge) syndrome? 12539040 2003
Entrez Id: 2034
Gene Symbol: EPAS1
EPAS1
0.200 Biomarker disease MGD Heterozygous deficiency of hypoxia-inducible factor-2alpha protects mice against pulmonary hypertension and right ventricular dysfunction during prolonged hypoxia. 12750401 2003
Entrez Id: 2034
Gene Symbol: EPAS1
EPAS1
0.200 Biomarker disease MGD Loss of HIF-2alpha and inhibition of VEGF impair fetal lung maturation, whereas treatment with VEGF prevents fatal respiratory distress in premature mice. 12053176 2002
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.200 Biomarker disease MGD Arteriolar and venular patterning in retinas of mice selectively expressing VEGF isoforms. 11827992 2002
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.200 Biomarker disease MGD Loss of HIF-2alpha and inhibition of VEGF impair fetal lung maturation, whereas treatment with VEGF prevents fatal respiratory distress in premature mice. 12053176 2002
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.200 Biomarker disease MGD Loss of the VEGF(164) and VEGF(188) isoforms impairs postnatal glomerular angiogenesis and renal arteriogenesis in mice. 12039984 2002
Entrez Id: 6441
Gene Symbol: SFTPD
SFTPD
0.200 Biomarker disease RGD Respiratory distress after intratracheal bleomycin: selective deficiency of surfactant proteins B and C. 11504697 2001
Entrez Id: 653509
Gene Symbol: SFTPA1
SFTPA1
0.200 Biomarker disease RGD Respiratory distress after intratracheal bleomycin: selective deficiency of surfactant proteins B and C. 11504697 2001
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
0.200 Biomarker disease MGD Defective heparan sulfate biosynthesis and neonatal lethality in mice lacking N-deacetylase/N-sulfotransferase-1. 10852901 2000
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
0.200 Biomarker disease MGD Targeted disruption of NDST-1 gene leads to pulmonary hypoplasia and neonatal respiratory distress in mice. 10664446 2000
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.200 Biomarker disease MGD Impaired myocardial angiogenesis and ischemic cardiomyopathy in mice lacking the vascular endothelial growth factor isoforms VEGF164 and VEGF188. 10229225 1999
Entrez Id: 3576
Gene Symbol: CXCL8
CXCL8
0.020 AlteredExpression disease BEFREE The effects of IL-10 on proinflammatory cytokine expression (IL-1beta and IL-8) in hyaline membrane disease (HMD). 9683557 1998
Entrez Id: 3576
Gene Symbol: CXCL8
CXCL8
0.020 AlteredExpression disease BEFREE Differential regulation of IL-8 by IL-1beta and TNFalpha in hyaline membrane disease. 9475356 1998
Entrez Id: 196
Gene Symbol: AHR
AHR
0.010 GeneticVariation disease BEFREE Home delivery (AHR = 2.25, 95% CI (1.03, 4.88)), hyaline membrane disease (AHR =3.21, 95% CI (1.96, 5.25)), gestational age, (AHR = 0.82, 95% CI (0.74, 0.91)), cry immediately at birth (AHR = 1.74, 95% CI (1.19, 2.53)), kangaroo mother care (AHR = 0.24, 95%CI (0.11, 0.52)), presence of jaundice (AHR = 1.62, 95%CI (1.12, 2.54)) and hypoglycemia at admission (AHR = 1.75, 95%CI (1.21, 2.54)) were found to be significant predictors of time to death for preterm neonates. 30616641 2019
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
0.010 Biomarker disease LHGDN Nuclear factor kappaB activation in pulmonary leukocytes from infants with hyaline membrane disease: associations with chorioamnionitis and Ureaplasma urealyticum colonization. 15746262 2005
Entrez Id: 3586
Gene Symbol: IL10
IL10
0.010 AlteredExpression disease BEFREE The effects of IL-10 on proinflammatory cytokine expression (IL-1beta and IL-8) in hyaline membrane disease (HMD). 9683557 1998