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
CAMRQ2 C567656
CAMRQ3 C567690
CANDF1 C567779
CANDF2 C537979
4p syndrome, chromosome D054877
CANDF3 C564361
CANDF4 C537979
CANDN1 C564361
CANOMAD syndrome C537980
4p syndromes, chromosome D054877
11 beta hydroxylase deficiency C535978
4p- syndrome D054877
ADVIRC C536352
CAPOS C535351
kidney diseases, cystic D052177