Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Purpura [NCBI]

Gene


 Gene Link Information
Gain		 01
TEC [NCBI] 0.000300643
PROC [NCBI] 3.41206e-05
TROVE2 [NCBI] 1.56953e-05
ST6GAL1 [NCBI] 1.13417e-05
SYK [NCBI] 1.03849e-05
CD36 [NCBI] 9.88044e-06
CCR4 [NCBI] 8.41562e-06
ITGB3 [NCBI] 7.62113e-06
GZMB [NCBI] 7.0479e-06
FOXP3 [NCBI] 6.3218e-06
CD68 [NCBI] 4.95768e-06
TNF [NCBI] 2.07468e-06



OMIM


 OMIM Link Information
gain		 01
pigmented purpuric eruption [NCBI] 0.00360325
reticuloendotheliosis, x-linked [NCBI] 0.00116675
thrombocytopenia, autosomal recessive [NCBI] 0.000773718
IGAN1 [NCBI] 0.000490783
protein c deficiency, congenital thrombotic disease due to [NCBI] 0.000183154
factor v deficiency [NCBI] 0.000108593
encephalopathy, ethylmalonic [NCBI] 0.000106243
LSA [NCBI] 6.54285e-05
thrombocytopenic purpura, autoimmune [NCBI] 6.3514e-05
PROS1 [NCBI] 5.5329e-05
WAS [NCBI] 4.15377e-05
CD [NCBI] 2.93071e-05
SLE [NCBI] 2.26105e-05
TNF [NCBI] 4.7112e-06



Database Center for Life Science