Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Arachnoid [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



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