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| created at |
2021-12-15 00:03:01 UTC |
| updated at |
2021-12-16 08:13:02 UTC |
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MeSH® Disease Terms
Source: ASCII MeSH files (d2022.bin and c2022.bin) downloaded from https://nlmpubs.nlm.nih.gov/projects/mesh/MESH_FILES/asciimesh/at Dec 14 16:16 (JST)
Method:
step1: Selected records that have tree numbers (MN) beginning with 'C' and took preferred term (MH) and synonyms (ENTRY and PRINT ENTRY: terms at the left of the first vertical bars), and the corresponding MeSH Unique IDs (UI) from the descriptor file (d2022.bin).
step2: Selected records that have corresponding descriptor (HM) that corresponds to an entry in step1, and took preferred term (NM) and synonyms (SY), and the corresponding MeSH Unique IDs (UI) from the supplementary records file (c2022.bin).
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80,878 entries
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There is 0 pattern entry.
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10q duplication syndrome
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C537804 |
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10q partial trisomy
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C537804 |
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10q- deletion
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C538289 |
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CMT 2b
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C537989 |
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11-beta-hydroxysteroid dehydrogenase, type i, deficiency of
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C536447 |
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11b hydroxylase deficiency
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C535978 |
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11p deletion syndrome
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C541598 |
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11p partial monosomy syndrome
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D017624 |
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11q deletion disorder
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D054868 |
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11q deletion syndrome
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D054868 |
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11q partial trisomy
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C538294 |
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11q terminal deletion disorder
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D054868 |
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11q- deletion syndrome
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D054868 |
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11q- deletion syndromes
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D054868 |
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11q23 deletion disorder
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D054868 |
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