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
CMT2C C565261
HMSN IIC C565261
HMSN2C C565261
axonal, autosomal dominant, type 2c charcot-marie-tooth disease C565261
charcot-marie-tooth disease, axonal, autosomal dominant, type 2c C565261
charcot-marie-tooth neuropathy, type 2c C565261
hereditary motor and sensory neuropathy, type IIC C565261
type 2c charcot-marie-tooth neuropathy C565261
type IIC hereditary motor and sensory neuropathy C565261