| 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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dominant hypercholesterolemia, autosomal
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D006938 |
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dominant hypercholesterolemias, autosomal
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D006938 |
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familial ligand defective apolipoprotein b 100
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D006938 |
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hyperlipoproteinemia, familial combined
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D006938 |
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hyperlipoproteinemias, familial combined
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D006938 |
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familial defective apolipoprotein b 100
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D006938 |
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familial defective apolipoprotein b-100
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D006938 |
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familial ligand-defective apolipoprotein b-100
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D006938 |
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combined hyperlipoproteinemia, familial
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D006938 |
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combined hyperlipoproteinemias, familial
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D006938 |
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hypercholesterolemic xanthomatoses, familial
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D006938 |
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hypercholesterolemic xanthomatosis, familial
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D006938 |
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apolipoprotein b-100, familial defective
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D006938 |
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apolipoprotein b-100, familial ligand-defective
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D006938 |
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lipoproteinemia, hyper-low density
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D006938 |
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