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
22q11.2 deletion syndrome D004062
22q11.2DS D004062
DiGeorge anomaly D004062
DiGeorge sequence D004062
DiGeorge syndrome D004062
VCF syndrome D004062
autosomal dominant opitz g bbb syndrome D004062
autosomal dominant opitz g-bbb syndrome D004062
catch22 D004062
conotruncal anomaly face syndrome D004062
conotruncal anomaly face syndrome (CTAF) D004062
deletion 22q11.2 syndrome D004062
deletion syndrome, 22q11.2 D004062
familial third and fourth pharyngeal pouch syndrome D004062
hypoplasia of thymus and parathyroids D004062