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
CLN3 related neuronal ceroid lipofuscinosis D009472
adult type neuronal ceroid lipofuscinosis D009472
kufs type neuronal ceroid lipofuscinosis D009472
late infantile neuronal ceroid lipofuscinosis D009472
ceroid lipofuscinosis, neuronal, 3 D009472
ceroid lipofuscinosis, neuronal, 4a, autosomal recessive D009472
ceroid lipofuscinosis, neuronal, 4b, autosomal dominant D009472
ceroid lipofuscinosis, neuronal, parry type D009472
disease, vogt spielmeyer D009472
disease, ceroid storage D009472
disease, lipofuscin storage D009472
neuronal, parry type ceroid lipofuscinosis D009472
spielmeyer disease, vogt D009472
batten spielmeyer vogt disease D009472