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
18-alpha hydroxylase deficiency C537806
18-hydroxylase deficiency C537806
18-oxidase deficiency C537806
CMO II deficiency C537806
CMO i deficiency C537806
aldosterone deficiency 1 C537806
aldosterone deficiency due to defect in 18-hydroxylase C537806
aldosterone deficiency type II C537806
aldosterone deficiency type i C537806
corticosterone methyloxidase type 1 deficiency C537806
corticosterone methyloxidase type II deficiency C537806
corticosterone methyloxidase type i deficiency C537806
familial, type i hyperreninemic hypoaldosteronism C537806
steroid 18-hydroxylase deficiency C537806
hyperreninemic hypoaldosteronism, familial, type i C537806