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
1 posterior polar cataract C535339
1 rippling muscle disease C535686
1 tremor familial essential C536545
1 tremor hereditary essential C536545
1, lissencephaly D054221
1, lissencephaly type D054221
1, preeclampsia eclampsia D011225
1, vesicoureteral reflux D014718
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine poisoning D020267
1-alpha, 25-hydroxyvitamin d3 deficiency, selective C562688
1-alpha-hydroxylase deficiency C562688
1-pyrroline-5-carboxylate dehydrogenase deficiency C538385
1.35-mb chromosome 1q21.1 deletion syndrome C567291
10p deletion syndrome (partial) C538288
10p- partial chromosome 10 C538288