| manager |
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| language |
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| license |
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| created at |
2021-12-23 02:14:06 UTC |
| updated at |
2021-12-23 14:43:01 UTC |
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"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
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82,725 entries
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There is 0 pattern entry.
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Gamma-sarcoglycanopathy
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C535900 |
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LGMD2C
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C535900 |
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SCARMD
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C535900 |
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maghrebian myopathy
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C535900 |
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limb-girdle, type 2c muscular dystrophy
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C535900 |
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muscular dystrophy, Duchenne-like
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C535900 |
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type 2c Limb-girdle muscular dystrophy
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C535900 |
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secondary adhalin deficiency
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C535900 |
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severe childhood autosomal recessive muscular dystrophy, north african type
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C535900 |
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autosomal recessive, type 1 Duchenne-like muscular dystrophy
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C535900 |
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adhalin deficiency, secondary
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C535900 |
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Duchenne-like muscular dystrophy
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C535900 |
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Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency
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C535900 |
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Duchenne-like muscular dystrophy, autosomal recessive, type 1
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C535900 |
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Limb-girdle muscular dystrophy, type 2c
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C535900 |
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