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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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Acyl-CoA dehydrogenase, very long-chain, deficiency of
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C536353 |
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Pearson's marrow-pancreas syndrome
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C536353 |
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VLCAD deficiency
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C536353 |
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acadvl
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C536353 |
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acyl-coa dehydrogenase very long chain deficiency
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C536353 |
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sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction
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C536353 |
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very long-chain acyl coenzyme a dehydrogenase deficiency
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C536353 |
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very long-chain acyl-CoA dehydrogenase deficiency
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C536353 |
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very long-chain acyl-coenzyme a dehydrogenase deficiency
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C536353 |
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very long-chain, deficiency of Acyl-CoA dehydrogenase
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C536353 |
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vlcad-c
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C536353 |
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vlcad-h
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C536353 |
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pearson marrow-pancreas syndrome
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C536353 |
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pearson syndrome
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C536353 |
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