Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Spinal Cord Neoplasms	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000348762
GFAP	[NCBI]	9.81406e-05
VUR	[NCBI]	5.24233e-05
VHL	[NCBI]	4.05307e-05
CD99	[NCBI]	2.0938e-05
EPB41L3	[NCBI]	2.04188e-05
SMARCB1	[NCBI]	1.52137e-05
NF1	[NCBI]	1.50912e-05
MEN1	[NCBI]	1.15964e-05
EPB41	[NCBI]	9.83367e-06
CXCR6	[NCBI]	8.1818e-06
EGFR	[NCBI]	7.95345e-06
CXCL16	[NCBI]	7.95106e-06
TNC	[NCBI]	7.80348e-06
KRIT1	[NCBI]	7.2324e-06
PTEN	[NCBI]	7.20619e-06
SDHD	[NCBI]	7.15342e-06
EPB41L2	[NCBI]	6.34142e-06
PIP	[NCBI]	6.28275e-06
BSG	[NCBI]	6.04645e-06
PAX3	[NCBI]	5.49623e-06
PCNA	[NCBI]	5.25628e-06
ABCG2	[NCBI]	4.77169e-06
ALK	[NCBI]	4.6724e-06
CDKN2B	[NCBI]	4.41007e-06
CDH1	[NCBI]	4.41007e-06
APC	[NCBI]	3.13356e-06
TG	[NCBI]	2.97968e-06
HRAS	[NCBI]	2.87041e-06
MBP	[NCBI]	2.33573e-06
PRL	[NCBI]	1.60343e-06
EGF	[NCBI]	9.41162e-07
TNF	[NCBI]	2.64082e-07

OMIM	Link	Information gain
angioma, hereditary neurocutaneous	[NCBI]	0.00206499
chiari malformation type i	[NCBI]	0.000626005
VHL	[NCBI]	0.000494826
GFAP	[NCBI]	0.000377093
meningioma, familial	[NCBI]	0.00021939
CCM	[NCBI]	0.0002056
RDT	[NCBI]	0.000187889
lipomyelomeningocele	[NCBI]	0.000131618
MUC1	[NCBI]	0.000116601
neurofibromatosis, familial spinal	[NCBI]	9.1078e-05
schwannomatosis	[NCBI]	7.58729e-05
lymphedema-distichiasis syndrome	[NCBI]	6.57736e-05
PGL1	[NCBI]	5.4453e-05
NF2	[NCBI]	4.84154e-05
NF1	[NCBI]	4.42191e-05
SDHD	[NCBI]	4.08564e-05
CD	[NCBI]	3.88292e-05
fragile x mental retardation syndrome	[NCBI]	3.34639e-05
RA	[NCBI]	3.28911e-05
DFSP	[NCBI]	2.80488e-05
AT	[NCBI]	2.29866e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency	[NCBI]	1.99936e-05
lymphoma, non-hodgkin, familial	[NCBI]	1.1014e-05
PCNA	[NCBI]	8.36155e-06
VEGF	[NCBI]	8.15099e-06
TG	[NCBI]	5.72124e-06
EGFR	[NCBI]	5.34975e-06
CEACAM5	[NCBI]	3.37621e-06
MBP	[NCBI]	2.98866e-06
TNF	[NCBI]	2.153e-06
PRL	[NCBI]	5.3714e-07
EGF	[NCBI]	6.66967e-08
KLK3	[NCBI]	2.52616e-08