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
CARASIL C563990
MAEDA syndrome C563990
nemoto disease C563990
familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension C563990
alopecia, and disc disease cerebrovascular disease with thin skin C563990
subcortical vascular encephalopathy, progressive C563990
cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy C563990
progressive subcortical vascular encephalopathy C563990
cerebrovascular disease with thin skin, alopecia, and disc disease C563990