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
schindler type neuronal axonal dystrophy C536631
type 1 Alpha-N-acetylgalactosaminidase deficiency C536631
type 1 schindler disease C536631
type 2 schindler disease C536631
type II NAGA deficiency C536631
type II alpha-N-Acetylgalactosaminidase deficiency C536631
type II schindler disease C536631
type III NAGA deficiency C536631
type III alpha-n-acetylgalactosaminidase deficiency C536631
type III schindler disease C536631
type i alpha-n-acetylgalactosaminidase deficiency C536631
type i naga deficiency C536631
type i schindler disease C536631
lysosomal glycoaminoacid storage disease-angiokeratoma corporis diffusum C536631