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| language |
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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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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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disorder, LDL receptor
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D006938 |
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disorders, LDL receptor
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D006938 |
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autosomal dominant, type b hypercholesterolemia
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D006938 |
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density lipoproteinemia, hyper-low
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D006938 |
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density lipoproteinemias, hyper-low
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D006938 |
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autosomal dominant hypercholesterolemia
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D006938 |
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autosomal dominant hypercholesterolemias
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D006938 |
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xanthomatoses, familial hypercholesterolemic
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D006938 |
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xanthomatosis, familial hypercholesterolemic
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D006938 |
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familial combined hyperlipoproteinemia
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D006938 |
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type 2, hyperlipoproteinemia
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D006938 |
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type II hyperlipoproteinemia
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D006938 |
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type IIa hyperlipoproteinemia
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D006938 |
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