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| created at |
2021-12-15 00:03:01 UTC |
| updated at |
2021-12-16 08:13:02 UTC |
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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).
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80,878 entries
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There is 0 pattern entry.
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18-alpha hydroxylase deficiency
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C537806 |
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18-hydroxylase deficiency
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C537806 |
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18-oxidase deficiency
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C537806 |
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CMO II deficiency
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C537806 |
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CMO i deficiency
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C537806 |
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aldosterone deficiency 1
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C537806 |
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aldosterone deficiency due to defect in 18-hydroxylase
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C537806 |
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aldosterone deficiency type II
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C537806 |
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aldosterone deficiency type i
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C537806 |
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corticosterone methyloxidase type 1 deficiency
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C537806 |
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corticosterone methyloxidase type II deficiency
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C537806 |
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corticosterone methyloxidase type i deficiency
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C537806 |
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familial, type i hyperreninemic hypoaldosteronism
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C537806 |
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steroid 18-hydroxylase deficiency
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C537806 |
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steroid 18-oxidase deficiency
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C537806 |
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