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
muscle-eye-brain disease, POMT1-Related D058494
muscle-eye-brain diseases D058494
muscle-eye-brain diseases, POMT1-Related D058494
muscular dystrophy due to defective glycosylation of dystroglycan 4a D058494
muscular dystrophy, fukuyama D058494
muscular dystrophy, limb-girdle, autosomal recessive, with mental retardation D058494
muscular dystrophy, limb-girdle, type 2k D058494
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 D058494
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 D058494
walker warburg syndrome D058494
pagon syndrome D058494
pagon syndromes D058494
syndrome, pagon D058494
syndrome, walker-warburg D058494
syndrome, warburg D058494