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
hypercholesterolemia, autosomal dominant, type b D006938
combined hyperlipoproteinemia, familial D006938
combined hyperlipoproteinemias, familial D006938
hypercholesterolemic xanthomatoses, familial D006938
hypercholesterolemic xanthomatosis, familial D006938
apolipoprotein b-100, familial defective D006938
apolipoprotein b-100, familial ligand-defective D006938
density lipoproteinemia, hyper-low D006938
density lipoproteinemias, hyper-low D006938
autosomal dominant hypercholesterolemia D006938
autosomal dominant hypercholesterolemias D006938
xanthomatoses, familial hypercholesterolemic D006938
xanthomatosis, familial hypercholesterolemic D006938
familial combined hyperlipoproteinemia D006938
type 2, hyperlipoproteinemia D006938