Mesh_All_FN Find_IDs Find_Terms Annotation
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created at 2021-12-23 02:14:06 UTC
updated at 2021-12-23 14:43:01 UTC
"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
82,725 entries
Label
Id
congenital fiber-type disproportions D020914
centronuclear, autosomal dominant myopathy D020914
disproportion, congenital fiber-type D020914
disproportions, congenital fiber-type D020914
congenital, with fiber-type disproportion myopathy D020914
tubular aggregate myopathies D020914
congenital non-progressive myopathies D020914
congenital structural myopathies D020914
structural, congenital myopathies D020914
x-linked centronuclear myopathies D020914
x-linked myotubular myopathies D020914
non progressive myopathies, congenital D020914
centronuclear, 1 myopathy D020914
congenital non-progressive myopathy D020914
congenital structural myopathy D020914