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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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dysmorphodystrophies, congenital mesodermal
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D056846 |
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dysmorphodystrophy, congenital mesodermal
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D056846 |
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marchesani weill syndrome
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D056846 |
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spherophakia brachymorphia syndrome
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D056846 |
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weill marchesani syndrome
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D056846 |
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weill marchesani syndrome, autosomal dominant
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D056846 |
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weill marchesani syndrome, autosomal recessive
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D056846 |
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spherophakia brachymorphia syndromes
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D056846 |
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autosomal dominant weill marchesani syndrome
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D056846 |
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autosomal recessive weill marchesani syndrome
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D056846 |
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autosomal dominant weill-marchesani syndrome
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D056846 |
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autosomal recessive weill-marchesani syndrome
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D056846 |
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