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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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inherited human disorders
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DISEASE |
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GI adverse experiences
|
DISEASE |
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malformed external ears
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DISEASE |
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inherited coagulation factor V deficiency
|
DISEASE |
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inherited coagulation factor v deficiency
|
DISEASE |
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deficiency of hepatic phenylalanine hydroxylase
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DISEASE |
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impaired memory functioning
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DISEASE |
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renal or hepatic toxicity
|
DISEASE |
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abnormal glucose homeostasis
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DISEASE |
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neuropathological disorder glaucoma
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DISEASE |
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LCD type i
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DISEASE |
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coloboma of iris and choroid
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DISEASE |
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Mendelian Inheritance in Man [MIM] 604367
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DISEASE |
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mendelian inheritance in man [MIM] 604367
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DISEASE |
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ischemic and haemorrhagic stroke
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DISEASE |
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