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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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7-dehydrocholesterol reductase deficiencies
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D019082 |
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7-dehydrocholesterol reductase deficiency
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D019082 |
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RSH SLO syndrome
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D019082 |
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RSH syndrome
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D019082 |
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RSH syndromes
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D019082 |
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RSH-SLO syndrome
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D019082 |
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RSH-SLO syndromes
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D019082 |
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SLO syndrome
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D019082 |
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SLO syndromes
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D019082 |
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acrodysgenital syndrome, lethal
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D019082 |
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acrodysgenital syndromes, lethal
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D019082 |
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deficiencies, 7-dehydrocholesterol reductase
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D019082 |
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deficiency, 7-dehydrocholesterol reductase
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D019082 |
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sex reversal, renal hypoplasia, and unilobar lung polydactyly
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D019082 |
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hyperotosis corticalis generalisata familiaris
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D019082 |
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