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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.
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schut-haymaker type OPCA
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D020754 |
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spinocerebellar ataxia, autosomal dominant, with sensory axonal neuropathy
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D020754 |
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dominantly-inherited spinocerebellar ataxia
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D020754 |
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spinocerebellar ataxia, cuban type
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D020754 |
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autosomal dominant cerebellar ataxia, type II
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D020754 |
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olivopontocerebellar atrophy, holguin type
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D020754 |
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spinocerebellar ataxias, dominantly inherited
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D020754 |
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spinocerebellar ataxia, dominantly-inherited
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D020754 |
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spinocerebellar ataxias, dominantly-inherited
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D020754 |
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OPCA with macular degeneration and external ophthalmoplegia
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D020754 |
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cerebelloparenchymal disorder is
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D020754 |
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olivopontocerebellar atrophy is
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D020754 |
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spinocerebellar atrophy is
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D020754 |
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cerebelloparenchymal disorder i
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D020754 |
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olivopontocerebellar atrophy i
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D020754 |
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