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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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spongy degeneration of the central nervous system
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D017825 |
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spongy degeneration of white matter in infancy
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D017825 |
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spongy disease of central nervous system
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D017825 |
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spongy disease of white matter
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D017825 |
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sporadic form canavan disease
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D017825 |
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sporadic form of canavan disease
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D017825 |
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syndrome, van bogaert-bertrand
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D017825 |
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type II canavan disease
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D017825 |
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type III canavan disease
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D017825 |
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type i canavan disease
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D017825 |
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van bogaert bertrand syndrome
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D017825 |
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van bogaert-bertrand syndrome
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D017825 |
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von bogaert bertrand disease
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D017825 |
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von bogaert-bertrand disease
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D017825 |
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leukodystrophy, spongiform
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D017825 |
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