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 beta-ol dehydrogenase deficiency C538236
3 methylcrotonylglycinuria C535308
3 methylglutaconic aciduria, type II D056889
3 methylglutaconicaciduria type 2 D056889
3 primary ciliary dyskinesia C535278
3, 3-prime, 4, associated with metacarpal and metatarsal synostoses synpolydactyly C564278
3-Hydroxy-2-Methylbutyryl-CoA dehydrogenase deficiency C564560
3-Hydroxy-3-Methylglutaryl-CoA lyase deficiency C538324
3-Hydroxy-3-Methylglutaryl-CoA synthase 2 deficiency C567784
3-Hydroxyacyl-CoA dehydrogenase II deficiency C564560
3-Hydroxyacyl-CoA dehydrogenase deficiency C535310
3-Hydroxyacyl-CoA dehydrogenase, long chain, deficiency C566945
3-Hydroxyacyl-CoA dehydrogenase, type 2, deficiency C564560
3-Hydroxyisobutyryl-CoA hydrolase deficiency C562803
3-Methylcrotonyl-CoA carboxylase 2 deficiency C535309