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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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inherited coagulation factor v deficiency
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DISEASE |
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Mendelian Inheritance in Man [MIM] 604367
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DISEASE |
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deficiency of hepatic phenylalanine hydroxylase
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DISEASE |
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renal or hepatic toxicity
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DISEASE |
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malformed external ears
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DISEASE |
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impaired memory functioning
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DISEASE |
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neuropathological disorder glaucoma
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DISEASE |
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mendelian inheritance in man [MIM] 604367
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DISEASE |
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congenital or infantile nephrotic syndrome
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DISEASE |
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myocardial energy metabolism disorder
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DISEASE |
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hypoxic-ischemic (HI) injury
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DISEASE |
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hypoxic-ischemic neuronal injury
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DISEASE |
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longer QT interval
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DISEASE |
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prolonged QTc interval
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DISEASE |
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intraventricular and intracerebral haemorrhage
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DISEASE |
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