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

There is 0 pattern entry.

Label
Id
adhalin deficiency, secondary C535900
north african type severe childhood autosomal recessive muscular dystrophy C535900
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