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
CAMRQ1 C535731
VLDLR associated cerebellar hypoplasia C535731
VLDLR-Associated cerebellar hypoplasia C535731
autosomal recessive cerebellar ataxia with mental retardation C535731
autosomal recessive cerebellar hypoplasia with cerebral gyral simplification C535731
cerebellar ataxia, congenital, and mental retardation, autosomal recessive C535731
cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1 C535731
cerebellar disorder, nonprogressive, with mental retardation C535731
cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion C535731
cerebellar hypoplasia, VLDLR associated C535731
cerebellar hypoplasia, VLDLR-Associated C535731
chmrq1 C535731
congenital, and mental retardation, autosomal recessive cerebellar ataxia C535731
des-vldlr C535731
dysequilibrium syndrome C535731