MeSH2022Disease Find_IDs Find_Terms Annotation
manager
language -
license -
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
ADVIRC C536352
autosomal dominant vitreoretinochoroidopathy C536352
autosomal dominant, with nanophthalmos vitreoretinochoroidopathy C536352
glaucoma, and cataract vitreoretinochoroidopathy with microcornea C536352
rod-cone dystrophy, cataract, and posterior staphyloma microcornea C536352
vitreoretinochoroidopathy C536352
vitreoretinochoroidopathy dominant C536352
vitreoretinochoroidopathy with microcornea, glaucoma, and cataract C536352
vitreoretinochoroidopathy, autosomal dominant C536352
vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos C536352
microcornea, rod-cone dystrophy, cataract, and posterior staphyloma C536352