Mesh_All_FN Find_IDs Find_Terms Annotation
manager
language -
license -
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
dominant hypercholesterolemia, autosomal D006938
dominant hypercholesterolemias, autosomal D006938
familial ligand defective apolipoprotein b 100 D006938
hyperlipoproteinemia, familial combined D006938
hyperlipoproteinemias, familial combined D006938
familial defective apolipoprotein b 100 D006938
familial defective apolipoprotein b-100 D006938
familial ligand-defective apolipoprotein b-100 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
lipoproteinemia, hyper-low density D006938