Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Neuraminic Acids [NCBI]

Gene


 Gene Link Information
Gain		 01
CMAH [NCBI] 0.000805241
SIGLECP3 [NCBI] 0.00018904
SIGLEC16 [NCBI] 0.000174209
TF [NCBI] 3.04614e-06
SIGLEC6 [NCBI] 2.6445e-06
SIGLEC12 [NCBI] 2.58118e-06
CMAS [NCBI] 2.5077e-06
SV2A [NCBI] 2.18022e-06
PCSK7 [NCBI] 2.174e-06
MASP1 [NCBI] 2.15046e-06
TGM3 [NCBI] 2.12369e-06
PCSK6 [NCBI] 2.06862e-06
CGA [NCBI] 2.02649e-06
ABO [NCBI] 1.92461e-06
FCN1 [NCBI] 1.9222e-06
SIGLEC1 [NCBI] 1.87203e-06
APOC3 [NCBI] 1.77476e-06
LTA [NCBI] 1.64318e-06
CD22 [NCBI] 1.63569e-06
PLG [NCBI] 1.58294e-06
AFP [NCBI] 1.05721e-06
EPO [NCBI] 9.92901e-07



OMIM


 OMIM Link Information
gain		 01
cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia [NCBI] 0.003491
CMAH [NCBI] 0.000640798
HAE [NCBI] 0.000296498
myopathy with storage of glycoproteins and glycosaminoglycans [NCBI] 0.000141951
THC2 [NCBI] 0.000109155
gm1-gangliosidosis, type ii [NCBI] 0.000103444
sialuria [NCBI] 0.000101821
mucolipidosis iiia [NCBI] 9.88885e-05
CLN1 [NCBI] 9.62935e-05
sialuria, finnish type [NCBI] 8.90247e-05
infantile sialic acid storage disorder [NCBI] 8.90247e-05
gm1-gangliosidosis, type i [NCBI] 8.73168e-05
mannosidosis, alpha b, lysosomal [NCBI] 7.9142e-05
sandhoff disease [NCBI] 7.69697e-05
NPC1 [NCBI] 6.88341e-05
giant platelet syndrome [NCBI] 5.73929e-05
TSD [NCBI] 4.53123e-05
CD22 [NCBI] 3.6576e-05
farber lipogranulomatosis [NCBI] 3.26603e-05
SN [NCBI] 3.01701e-05
EPB41 [NCBI] 3.01701e-05
ORM1 [NCBI] 2.9927e-05
C1NH [NCBI] 2.83003e-05
TF [NCBI] 2.79716e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 2.57131e-05
F2 [NCBI] 2.44684e-05
FGA [NCBI] 2.27358e-05
PAEP [NCBI] 2.17292e-05
HEMB [NCBI] 1.8597e-05
PI [NCBI] 1.58296e-05
MAG [NCBI] 1.36361e-05
AFP [NCBI] 5.0046e-06
EPO [NCBI] 3.95889e-06
CEACAM5 [NCBI] 3.11125e-06
CF [NCBI] 1.9983e-06



Database Center for Life Science