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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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ACCPN
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C536446 |
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agenesis of corpus callosum with neuronopathy
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C536446 |
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agenesis of corpus callosum with peripheral neuropathy
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C536446 |
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agenesis of corpus callosum with polyneuropathy
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C536446 |
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agenesis of the corpus callosum with peripheral neuropathy
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C536446 |
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agenesis of, with neuronopathy corpus callosum
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C536446 |
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andermann syndrome
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C536446 |
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charlevoix disease
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C536446 |
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corpus callosum agenesis neuronopathy
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C536446 |
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corpus callosum, agenesis of, with neuronopathy
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C536446 |
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hereditary motor and sensory neuropathy with agenesis of the corpus callosum
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C536446 |
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polyneuropathy, sensorimotor, with or without agenesis of the corpus callosum
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C536446 |
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sensorimotor, with or without agenesis of the corpus callosum polyneuropathy
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C536446 |
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