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MeSH keywords -> Related genes, diseases (OMIM)


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01 Prosopagnosia [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
prosopagnosia, hereditary [NCBI] 0.00243653
AD [NCBI] 7.32933e-05
FTD [NCBI] 4.47381e-05
panencephalitis, subacute sclerosing [NCBI] 4.42993e-05




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