MeSH2022Disease (80,878) Find_IDs Annotation
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created at 2021-12-15 00:03:01 UTC
updated at 2021-12-16 08:13:02 UTC
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).
Label
Id
CMT 2k C535418
Cmt2k C535418
axonal, autosomal recessive, type 2k charcot-marie-tooth disease C535418
axonal, type 2k charcot-marie-tooth disease C535418
axonal, type 2k charcot-marie-tooth neuropathy C535418
charcot-marie-tooth disease, axonal, autosomal recessive, type 2k C535418
charcot-marie-tooth disease, axonal, type 2k C535418
charcot-marie-tooth disease, type 2k C535418
charcot-marie-tooth neuropathy, axonal, type 2k C535418
type 2k charcot-marie-tooth disease C535418