Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Pulmonary Atelectasis [NCBI]

Gene


 Gene Link Information
Gain		 01
DNASE1 [NCBI] 0.000170737
GER [NCBI] 0.000158688
HS3ST5 [NCBI] 2.39752e-05
SIM1 [NCBI] 1.15809e-05
NKX2-1 [NCBI] 6.18876e-06
ENG [NCBI] 5.78515e-06
ADA [NCBI] 4.79674e-06
TNF [NCBI] 4.40185e-06
MPO [NCBI] 3.07382e-06
EGF [NCBI] 2.11043e-06



OMIM


 OMIM Link Information
gain		 01
diaphragmatic hernia, congenital [NCBI] 0.000938218
CF [NCBI] 9.72217e-05
cutis laxa, autosomal recessive, type i [NCBI] 8.92647e-05
NDST1 [NCBI] 6.95919e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 6.90675e-05
SIM2 [NCBI] 6.6922e-05
PROP1 [NCBI] 5.86684e-05
ADA [NCBI] 2.19845e-05
TNF [NCBI] 1.89009e-05
MPO [NCBI] 1.25029e-05
EGF [NCBI] 7.16328e-06
SLE [NCBI] 2.60547e-07



Database Center for Life Science