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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hyaline Membrane Disease [NCBI]

Gene


 Gene Link Information
Gain		 01
SFTPA1B [NCBI] 1.02824e-05
DMBT1 [NCBI] 1.01952e-05
TIMP1 [NCBI] 8.61002e-06
SCGB1A1 [NCBI] 7.55481e-06
NKX2-1 [NCBI] 7.13349e-06
MMP2 [NCBI] 6.78462e-06
NFKB1 [NCBI] 6.60251e-06
MMP9 [NCBI] 6.40094e-06
IL10 [NCBI] 5.50342e-06
AVP [NCBI] 4.9459e-06
IL1RN [NCBI] 4.64973e-06
VWF [NCBI] 4.08544e-06
MPO [NCBI] 3.97802e-06
AFP [NCBI] 3.94514e-06
PRL [NCBI] 3.77837e-06
EGF [NCBI] 2.97372e-06



OMIM


 OMIM Link Information
gain		 01
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000814853
kniest-like dysplasia, lethal [NCBI] 0.000160393
vascular hyalinosis [NCBI] 0.000160393
kniest dysplasia [NCBI] 0.000100846
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome [NCBI] 9.52359e-05
CES [NCBI] 8.03246e-05
IL10 [NCBI] 4.98781e-05
AVP [NCBI] 1.76556e-05
MPO [NCBI] 1.52803e-05
AFP [NCBI] 1.49937e-05
PRL [NCBI] 1.36424e-05
EGF [NCBI] 9.65889e-06



Database Center for Life Science