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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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rutledge friedman harrod syndrome
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D019082 |
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rutledge lethal multiple congenital anomaly syndrome
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D019082 |
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hyperotosis corticalis generalisata familiaris
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D019082 |
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reductase deficiencies, 7-dehydrocholesterol
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D019082 |
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reductase deficiency, 7-dehydrocholesterol
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D019082 |
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syndrome, RSH
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D019082 |
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syndromes, RSH
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D019082 |
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syndromes, SLO
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D019082 |
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smith lemli opitz syndrome
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D019082 |
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smith lemli opitz syndrome, type 1
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D019082 |
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smith lemli opitz syndrome, type 2
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D019082 |
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smith lemli opitz syndrome, type II
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D019082 |
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smith lemli opitz syndrome, type i
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D019082 |
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smith-lemli-opitz syndrome
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D019082 |
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smith-lemli-opitz syndrome, type 1
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D019082 |
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