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
neuronal ceroid-lipofuscinosis D009472
santavuori-haltia disease D009472
spielmeyer-sjogren disease D009472
spielmeyer-vogt disease D009472
vogt-spielmeyer disease D009472
neuronal ceroid-lipofuscinoses, CLN3-Related D009472
neuronal ceroid-lipofuscinosis, CLN3-Related D009472
kufs disease, autosomal dominant D009472
amaurotic idiocy, adult type D009472
adult type amaurotic idiocy D009472
neuronal, 4b, autosomal dominant ceroid lipofuscinosis D009472
kufs disease autosomal recessive D009472
kufs disease, autosomal recessive D009472
neuronal, 4a, autosomal recessive ceroid lipofuscinosis D009472
disease, juvenile batten D009472