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
deficiencies, cerebroside sulfatase D007966
deficiency, ARSA D007966
deficiency, arylsulfatase a D007966
deficiency, cerebroside sulfatase D007966
diffuse, metachromatic form cerebral sclerosis D007966
greenfield disease D007966
infant metachromatic leukodystrophies D007966
infant metachromatic leukodystrophy D007966
infant type metachromatic leukodystrophy D007966
infant-type metachromatic leukodystrophies D007966
infant-type metachromatic leukodystrophy D007966
juvenile metachromatic leukodystrophies D007966
juvenile metachromatic leukodystrophy D007966
juvenile type metachromatic leukodystrophy D007966
juvenile-type metachromatic leukodystrophies D007966