MeSH2022Disease Find_IDs Find_Terms 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).
80,878 entries
Label
Id
1, lissencephaly D054221
1, lissencephaly type D054221
1s, lissencephaly D054221
1s, lissencephaly type D054221
agyria pachygyria band spectrum D054221
agyria-pachygyria-band spectrum D054221
band heterotopia, lissencephaly-subcortical D054221
chromosome 17p13.3 deletion syndrome D054221
classic lissencephalies D054221
classic lissencephaly D054221
classical lissencephalies D054221
classical lissencephalies and subcortical band heterotopias D054221
classical lissencephaly D054221
classical lissencephaly syndrome D054221
classical lissencephaly syndromes D054221