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
ADHCAI C562880
hypomineralization type amelogenesis imperfecta C562880
type III amelogenesis imperfecta C562880
amelogenesis imperfecta, hypocalcification type, autosomal dominant C562880
hypocalcification type, autosomal dominant amelogenesis imperfecta C562880
amelogenesis imperfecta, hypomineralization type C562880
amelogenesis imperfecta, type III C562880