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language |
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created at |
2021-12-23 00:44:09 UTC |
updated at |
2021-12-23 01:31:33 UTC |
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"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
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82,788 entries
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There is 0 pattern entry.
type 6 spinocerebellar ataxia
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D020754 |
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type 7 spinocerebellar ataxia
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D020754 |
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dominantly inherited spinocerebellar ataxias
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D020754 |
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spinocerebellar ataxia type 4
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D020754 |
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spinocerebellar ataxia type 5
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D020754 |
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spinocerebellar ataxia type 6
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D020754 |
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spinocerebellar ataxia type 7
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D020754 |
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OPCA, schut-haymaker type
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D020754 |
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spinocerebellar ataxia type 1
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D020754 |
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spinocerebellar ataxia type 2
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D020754 |
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schut haymaker type OPCA
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D020754 |
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swami syndrome, wadia
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D020754 |
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autosomal dominant, with sensory axonal neuropathy spinocerebellar ataxia
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D020754 |
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cerebellar degeneration with slow eye movements
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D020754 |
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spinocerebellar ataxia with slow eye movements
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D020754 |
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