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
DFNA17 C535507
Fechtner's syndrome C535507
MYH9 gene-related autosomal macrothrombocytopenias C535507
MYH9-Related disease C535507
MYH9-Related disorders C535507
MYH9RD C535507
alport syndrome with leukocyte inclusions and macrothrombocytopenia C535507
alport syndrome with macrothrombocytopenia C535507
autosomal dominant 17 deafness C535507
autosomal dominant myh9 spectrum disorders C535507
deafness, autosomal dominant 17 C535507
dohle leukocyte inclusions with giant platelets C535507
epstein syndrome C535507
fechtner syndrome C535507
myh9-related disorder C535507