Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Pulmonary Atelectasis	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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