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
juvenile-type metachromatic leukodystrophy D007966
sulfatase deficiencies, cerebroside D007966
sulfatase deficiency, cerebroside D007966
sulfatide lipidosis D007966
late infantile metachromatic leukodystrophy D007966
leukodystrophies, adult metachromatic D007966
leukodystrophies, adult-type metachromatic D007966
leukodystrophies, juvenile metachromatic D007966
leukodystrophies, juvenile-type metachromatic D007966
leukodystrophies, metachromatic D007966
leukodystrophy, adult metachromatic D007966
leukodystrophy, adult-type metachromatic D007966
leukodystrophy, juvenile metachromatic D007966
leukodystrophy, juvenile-type metachromatic D007966
leukodystrophy, metachromatic D007966