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
46,XY disorder of sex development due to LH defects C562567
46,XY disorders of sex development D058490
46,XY gonadal dysgenesis D006061
46,XY gonadal dysgenesis, complete or partial, DHH-Related C565537
46,XY gonadal dysgenesis, complete or partial, with or without adrenal failure D058490
46,XY sex reversal 3 D058490
46,XY sex reversal 4 C567887
46,XY sex reversal, partial or complete, NR5A1-Related D058490
46,xx gonadal dysgenesis, partial or complete, autosomal C567597
46,xy gonadal dysgenesis, complete or partial, with 9p24.3 deletion C567887
46,xy gonadal dysgenesis, complete, cbx2-related C567766
46,xy gonadal dysgenesis, complete, sry-related C567574
46,xy gonadal dysgenesis, partial, with minifascicular neuropathy C567773
46,xy true hermaphroditism, sry-related C567575
46,xy, cbx2-related disorder of sex development C567766