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
cerebroocular dysplasia-muscular dystrophy syndrome D058494
chemke syndrome D058494
congenital muscular dystrophy dystroglycanopathy with brain and eye anomalies, type a1 D058494
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type a1 D058494
disease, POMT1-Related muscle-eye-brain D058494
dystrophy, fukuyama muscular D058494
fktn related walker warburg syndrome D058494
fktn-related walker-warburg syndrome D058494
fktn-related walker-warburg syndromes D058494
fukuyama CMD D058494
fukuyama muscular dystrophy D058494
fukuyama syndrome D058494
hydrocephalus, agyria, and retinal dysplasia D058494
syndrome, COD-MD D058494
pagon syndrome D058494