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
11p partial monosomy syndrome D017624
WAGR complex D017624
WAGR complices D017624
WAGR contiguous gene syndrome D017624
WAGR syndrome D017624
WAGR syndromes D017624
aniridia, genitourinary anomalies, and mental retardation syndrome wilms tumor D017624
chromosome 11p13 deletion syndrome D017624
complex, WAGR D017624
aniridia, genitourinary anomalies, mental retardation syndrome wilms tumor D017624
wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome D017624
wilms tumor-aniridia-genital anomalies-retardation syndrome D017624
syndrome, WAGR D017624
wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome D017624
contiguous gene syndrome, WAGR D017624