MeSH2022Disease Find_IDs Find_Terms Annotation
manager
language -
license -
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
CCDS1 C535598
Slc6a8 deficiency C535598
Slc6a8-Related creatine transporter deficiency C535598
X-linked creatine deficiency C535598
X-linked creatine deficiency syndrome C535598
X-linked creatine transporter deficiency C535598
X-linked, with creatine transport deficiency mental retardation C535598
cerebral creatine deficiency syndrome 1 C535598
creatine deficiency syndrome, x-linked C535598
creatine deficiency, X-linked C535598
creatine transporter defect C535598
creatine transporter deficiency C535598
x-linked creatine deficiency C535598
x-linked creatine deficiency syndrome C535598
x-linked, with seizures, short stature, and midface hypoplasia mental retardation C535598