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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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11-Beta-hydroxylase deficiency
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C535978 |
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11 beta hydroxylase deficiency
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C535978 |
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11b hydroxylase deficiency
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C535978 |
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CYP11B1 deficiency congenital
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C535978 |
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adrenal hyperplasia 4
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C535978 |
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adrenal hyperplasia IV
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C535978 |
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adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency
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C535978 |
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adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency
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C535978 |
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adrenal hyperplasia, hypertensive form
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C535978 |
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congenital CYP11B1 deficiency
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C535978 |
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congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
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C535978 |
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congenital adrenal hyperplasia type 4
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C535978 |
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congenital, due to 11-Beta-hydroxylase deficiency adrenal hyperplasia
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C535978 |
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congenital, due to steroid 11-beta-hydroxylase deficiency adrenal hyperplasia
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C535978 |
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hypertensive form adrenal hyperplasia
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C535978 |
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