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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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hereditary, spastic paraplegia, autosomal dominant
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D015419 |
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hereditary, spastic paraplegia, x-linked recessive
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D015419 |
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hereditary, x-linked recessive spastic paraplegia
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D015419 |
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hypertrophic motor sensory neuropathy spastic paraplegia
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D015419 |
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hypertrophic motor-sensory neuropathy-spastic paraplegia
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D015419 |
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paraplegia, hereditary spastic
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D015419 |
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paraplegia, spastic, hereditary
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D015419 |
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paraplegias, hereditary spastic
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D015419 |
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peroneal muscular atrophy with pyramidal features, autosomal dominant
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D015419 |
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spastic paraplegia 2
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D015419 |
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spastic paraplegia hypertrophic motor sensory neuropathy
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D015419 |
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spastic paraplegia type 2
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D015419 |
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spastic paraplegia, autosomal dominant hereditary
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D015419 |
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spastic paraplegia, autosomal dominant, hereditary
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D015419 |
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spastic paraplegia, autosomal recessive, hereditary
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D015419 |
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