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
3-methylglutaconic aciduria, type III C535311
3-methylglutaconic aciduria, type i C562801
3-methylglutaconic aciduria, type v C565706
3-methylglutaconicaciduria type 2 D056889
3-methylglutaconicaciduria type 2s D056889
3-methylglutaconicaciduria type II D056889
3-methylglutaconicaciduria type IIs D056889
3-methylhydroxybutyric acidemia C535434
3-oxoacid coa transferase deficiency C537527
3-oxothiolase deficiency C535434
3b-Hydroxysteroid dehydrogenase deficiency C538236
3beta-Hsd deficiency C538236
3beta-Hsd deficiency congenital adrenal hyperplasia C538236
3beta-Hydroxysteroid dehydrogenase deficiency C538236
3c syndrome C535313