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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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12p monosomy, partial
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C538302 |
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12p trisomy chromosome 12
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C538299 |
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13q deletion syndrome
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C535484 |
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13q- syndrome, partial
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C535449 |
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15q11.2 microdeletion
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C557830 |
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15q13.3 microdeletion
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C567439 |
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15q13.3 microdeletion syndrome
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C567439 |
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15q24 deletion
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C579849 |
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15q24 microdeletion
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C579849 |
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15q24 microdeletion syndrome
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C579849 |
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16p11.2 deletion syndrome
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C579850 |
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16q22-Linked spinocerebellar ataxia
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C566146 |
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17 Beta-hydroxysteroid dehydrogenase deficiency
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C537805 |
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17 alpha ketosteroid reductase deficiency of testis
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C537805 |
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17,20-lyase deficiency, isolated
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C567076 |
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