MeSH2022Disease (80,878) Find_IDs 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).
Label
Id
DHMNVP C563562
HMN VIIA C563562
HMN7A C563562
distal hereditary motor, type VIIA neuropathy C563562
distal, with vocal cord paralysis spinal muscular atrophy C563562
harper-young myopathy C563562
neuropathy, distal hereditary motor, type VIIA C563562
spinal muscular atrophy, distal, with vocal cord paralysis C563562