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
BOF syndrome D019280
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging D019280
branchio oculo facial syndrome D019280
branchio oto renal syndrome D019280
branchio-oto-renal syndrome D019280
branchio-otorenal syndrome D019280
branchiooculofacial syndrome D019280
branchiootorenal dysplasia D019280
branchiootorenal syndrome 1 D019280
branchiootorenal syndrome 2 D019280
dysplasia, branchiootorenal D019280
growth retardation, imperforate nasolacrimal duct, and premature aging branchial clefts with characteristic facies D019280
hemangiomatous branchial clefts lip pseudocleft syndrome D019280
hemangiomatous branchial clefts-lip pseudocleft syndrome D019280
lee root fenske syndrome D019280