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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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charcot marie tooth disease with pyramidal features, autosomal dominant
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D015419 |
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charcot-marie-tooth disease with pyramidal features, autosomal dominant
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D015419 |
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hereditary autosomal dominant spastic paraplegia
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D015419 |
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hereditary autosomal recessive spastic paraplegia
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D015419 |
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hereditary motor and sensory neuropathy 5
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D015419 |
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hereditary motor and sensory neuropathy v
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D015419 |
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hereditary motor sensory neuropathy with pyramidal signs
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D015419 |
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hereditary motor-sensory neuropathy with pyramidal signs
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D015419 |
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hereditary spastic paraplegia
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D015419 |
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hereditary spastic paraplegia, autosomal recessive
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D015419 |
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hereditary spastic paraplegias
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D015419 |
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hereditary x linked recessive spastic paraplegia
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D015419 |
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hereditary x-linked recessive spastic paraplegia
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D015419 |
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hereditary, autosomal dominant spastic paraplegia
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D015419 |
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hereditary, autosomal recessive spastic paraplegia
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D015419 |
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