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| language |
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| license |
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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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LOCAH
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C535979 |
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NCCAH
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C535979 |
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21-hydroxylase deficiency
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C535979 |
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CYP21 deficiency
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C535979 |
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Late-onset congenital adrenal hyperplasia
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C535979 |
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attenuated congenital adrenal hyperplasia
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C535979 |
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21 hydroxylase deficiency
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C535979 |
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21 alpha hydroxylase deficiency
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C535979 |
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congenital adrenal hyperplasia 1
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C535979 |
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congenital adrenal hyperplasia due to 21 hydroxylase deficiency
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C535979 |
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adrenal hyperplasia III
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C535979 |
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non classic congenital adrenal hyperplasia
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C535979 |
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