MeSH2022Disease Find_IDs Find_Terms Annotation
manager
language -
license -
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
Acetazolamide-responsive episodic ataxia syndrome C535506
Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia C535506
Acetyl-CoA:alpha-Glucosaminide n-acetyltransferase deficiencies D009084
Acetyl-CoA:alpha-Glucosaminide n-acetyltransferase deficiency D009084
Acetyl-coa acetyltransferase 2 deficiency C536005
Acro-dermato-ungual-lacrimal-tooth syndrome C538052
Acro-osteolysis-facial dysplasia syndrome C536526
Acro-renal-uterine-mandibular syndrome C535665
Acyl-CoA dehydrogenase family, member 8, deficiency of C535541
Acyl-CoA dehydrogenase family, member 9, deficiency of C567006
Acyl-CoA dehydrogenase, medium chain, deficiency of C536038
Acyl-CoA dehydrogenase, very long-chain, deficiency of C536353
Addison's disease D000224
Addison's disease, myxedema diabetes mellitus D016884
Adie's pupil D015845