Disease_Mesh_All Find_IDs Find_Terms Annotation
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created at 2021-12-23 00:44:09 UTC
updated at 2021-12-23 01:31:33 UTC
"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
82,788 entries
Label
Id
type 6 spinocerebellar ataxia D020754
type 7 spinocerebellar ataxia D020754
dominantly inherited spinocerebellar ataxias D020754
spinocerebellar ataxia type 4 D020754
spinocerebellar ataxia type 5 D020754
spinocerebellar ataxia type 6 D020754
spinocerebellar ataxia type 7 D020754
OPCA, schut-haymaker type D020754
spinocerebellar ataxia type 1 D020754
spinocerebellar ataxia type 2 D020754
schut haymaker type OPCA D020754
swami syndrome, wadia D020754
autosomal dominant, with sensory axonal neuropathy spinocerebellar ataxia D020754
cerebellar degeneration with slow eye movements D020754
spinocerebellar ataxia with slow eye movements D020754