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
myopathy, CPEO with D007625
mitochondrial cytopathies, kearns-sayre D007625
mitochondrial cytopathy, kearn-sayre D007625
mitochondrial cytopathy, kearns-sayre D007625
pigmentary degeneration of retina, and cardiomyopathy ophthalmoplegia D007625
sayre syndrome, kearns D007625
syndrome, kearns D007625
syndrome, kearns sayre D007625
syndrome, kearns' D007625
syndrome, kearns-sayre D007625
syndrome, kearns-sayre-shy-daroff D007625
syndrome, oculocraniosomatic D007625
syndrome, ophthalmoplegia plus D007625
syndrome, ophthalmoplegia-plus D007625
syndromes, ophthalmoplegia-plus D007625