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
5-oxoprolinemia C536835
5-oxoprolinuria C536835
deficiency of glutathione synthase C536835
deficiency of glutathione synthetase C536835
hemolytic anemia due to glutathione synthetase deficiency of erythrocytes C536835
pyroglutamic acidemia C536835
pyroglutamic aciduria C536835
glutathione synthetase deficiency C536835
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to C536835