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| language |
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| license |
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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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cerebellar hypoplasia, nonprogressive norman type
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C565865 |
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CPD3
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C565865 |
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SCAR2
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C565865 |
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CPD III
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C565865 |
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autosomal recessive 2 spinocerebellar ataxia
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C565865 |
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spinocerebellar ataxia autosomal recessive 2
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C565865 |
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cerebelloparenchymal disorder III
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C565865 |
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spinocerebellar ataxia, autosomal recessive 2
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C565865 |
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congenital cerebellar granular cell hypoplasia and mental retardation
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C565865 |
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cerebellar granular cell hypoplasia and mental retardation, congenital
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C565865 |
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nonprogressive norman type cerebellar hypoplasia
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C565865 |
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