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
batten mayou disease D009472
batten spielmeyer vogt disease D009472
batten-mayou disease D009472
batten-spielmeyer-vogt disease D009472
cerebroretinal degeneration, juvenile D009472
cerebroretinal degenerations, juvenile D009472
ceroid lipofuscinosis, neuronal D009472
ceroid lipofuscinosis, neuronal 3, juvenile D009472
ceroid lipofuscinosis, neuronal 4 D009472
ceroid lipofuscinosis, neuronal, 3 D009472
ceroid lipofuscinosis, neuronal, 4a, autosomal recessive D009472
ceroid lipofuscinosis, neuronal, parry type D009472
ceroid storage disease D009472
ceroid storage diseases D009472
ceroid-lipofuscinosis, CLN3-Related neuronal D009472