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

There is 0 pattern entry.

Label
Id
BAFME2 C564313
FAME2 C564313
autosomal dominant cortical myoclonus and epilepsy C564313
benign adult familial myoclonic epilepsy 2 C564313
cortical myoclonus and epilepsy, autosomal dominant C564313
epilepsy, familial adult myoclonic 2 C564313
epilepsy, myoclonic, benign adult familial, type 2 C564313
familial adult myoclonic 2 epilepsy C564313
myoclonic, benign adult familial, type 2 epilepsy C564313
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