Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Arachnoid	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	8.69867e-05
FOXC1	[NCBI]	1.31141e-05
DSP	[NCBI]	1.14336e-05
CST3	[NCBI]	9.69496e-06
GJB2	[NCBI]	9.44923e-06
CTF1	[NCBI]	7.72876e-06
CD68	[NCBI]	7.24224e-06
YY1AP1	[NCBI]	6.89281e-06
PKP2	[NCBI]	6.81997e-06
PTGDS	[NCBI]	6.6885e-06
DSC3	[NCBI]	6.65817e-06
YAP1	[NCBI]	6.39673e-06
DSC2	[NCBI]	6.3087e-06
CADM1	[NCBI]	6.08331e-06
DSG2	[NCBI]	6.05023e-06
NF2	[NCBI]	5.80608e-06
CCNE1	[NCBI]	5.36927e-06
MSLN	[NCBI]	5.26027e-06
GJA1	[NCBI]	4.99049e-06
SELPLG	[NCBI]	4.075e-06
CCR7	[NCBI]	4.04197e-06
COMT	[NCBI]	3.91419e-06
BMP2	[NCBI]	2.98582e-06
APOE	[NCBI]	2.90877e-06
VWF	[NCBI]	2.65696e-06
TH	[NCBI]	1.95318e-06
PRL	[NCBI]	1.86228e-06

OMIM	Link	Information gain
hemophagocytic lymphohistiocytosis, familial, 1	[NCBI]	0.00199615
spinal arachnoiditis	[NCBI]	0.0017631
arachnoid cysts, intracranial	[NCBI]	0.000390315
melanosis, neurocutaneous	[NCBI]	0.000365873
amyloidosis vi	[NCBI]	0.000326873
MFS	[NCBI]	0.000263793
lymphedema-distichiasis syndrome	[NCBI]	0.000254733
spinal intradural arachnoid cysts	[NCBI]	0.000221495
intracranial hypertension, idiopathic	[NCBI]	0.000182229
amyloidosis vii	[NCBI]	0.000126664
hurler syndrome	[NCBI]	9.01537e-05
fabry disease	[NCBI]	7.0066e-05
DSC3	[NCBI]	4.71224e-05
DSC2	[NCBI]	4.49449e-05
DSG2	[NCBI]	4.3276e-05
temporal arteritis	[NCBI]	4.29725e-05
tay-sachs disease, ab variant	[NCBI]	4.19225e-05
FOXC1	[NCBI]	4.15226e-05
AT	[NCBI]	4.13695e-05
AD	[NCBI]	3.05912e-05
GJB2	[NCBI]	2.92982e-05
CEACAM5	[NCBI]	2.7819e-05
GJA1	[NCBI]	2.0521e-05
TTR	[NCBI]	2.00329e-05
COMT	[NCBI]	1.89376e-05
MUC1	[NCBI]	1.88419e-05
APOE	[NCBI]	1.19881e-05
KLK3	[NCBI]	1.03812e-05
SLE	[NCBI]	6.96067e-06
TH	[NCBI]	4.72994e-06
PRL	[NCBI]	4.2328e-06
VEGF	[NCBI]	1.3573e-06