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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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type i congenital antithrombin deficiency
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DISEASE |
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autosomal dominant congenital nuclear cataract
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DISEASE |
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autosomal dominant congenital nuclear lactescent cataract
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DISEASE |
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Scleroderma renal crisis
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DISEASE |
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scleroderma renal crisis
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DISEASE |
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renal tissue damage
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DISEASE |
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respiratory growth defect
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DISEASE |
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autosomal dominant defects
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DISEASE |
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congenital FV deficiency
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DISEASE |
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congenital antithrombin deficiency
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DISEASE |
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isolated pituitary deficiency
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DISEASE |
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mitochondrial DNA depletion
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DISEASE |
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apoptosis and deterioration of renal function
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DISEASE |
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abnormal limb development
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DISEASE |
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impaired intellectual development
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DISEASE |
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