Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
hemophagocytic lymphohistiocytosis, familial, 1 [NCBI] 0.0159475
letterer-siwe disease [NCBI] 0.00117822
histiocytosis, familial lipochrome [NCBI] 0.000938218
reticuloendotheliosis, x-linked [NCBI] 0.000938218
omenn syndrome [NCBI] 0.000524429
sea-blue histiocyte disease [NCBI] 0.000313496
histiocytosis, progressive mucinous [NCBI] 0.000115876
histiocytic dermatoarthritis [NCBI] 0.000115876
kindler syndrome [NCBI] 8.25826e-05
CSF1R [NCBI] 7.34161e-05
cerebrotendinous xanthomatosis [NCBI] 6.68256e-05
TGD [NCBI] 6.48401e-05
CGD [NCBI] 5.08554e-05
hla-d histocompatibility type [NCBI] 4.2561e-05
thrombocytopenic purpura, autoimmune [NCBI] 4.10122e-05
WAS [NCBI] 3.03253e-05
MUC1 [NCBI] 3.01679e-05
GFAP [NCBI] 1.98624e-05
RA [NCBI] 1.46004e-05



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