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
keller syndrome C537923
FG syndrome C537923
FG syndrome 1 C537923
FG syndrome 2 C537923
FG syndrome 3 C537923
FG syndrome 4 C537923
FGS1 C537923
opitz-kaveggia syndrome C537923
x-linked, cask-related mental retardation C537923
x-linked, with nystagmus mental retardation C537923
large head, imperforate anus, congenital hypotonia, and partial agenesis of the corpus callosum mental retardation C537923
mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of the corpus callosum C537923
mental retardation, x-linked, cask-related C537923
mental retardation, x-linked, with nystagmus C537923