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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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3-methylglutaconic aciduria, type III
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C535311 |
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OPA3, autosomal recessive
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C535311 |
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autosomal recessive OPA3
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C535311 |
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autosomal recessive optic atrophy 3
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C535311 |
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costeff optic atrophy syndrome
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C535311 |
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costeff syndrome
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C535311 |
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iraqi jewish optic atrophy plus
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C535311 |
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type III 3-methylglutaconic aciduria
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C535311 |
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infantile, with chorea and spastic paraplegia optic atrophy
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C535311 |
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optic atrophy 3, autosomal recessive
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C535311 |
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optic atrophy plus syndrome
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C535311 |
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optic atrophy, infantile, with chorea and spastic paraplegia
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C535311 |
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