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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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46,XY disorder of sex development due to LH defects
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C562567 |
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LH resistance due to LH receptor deactivation
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C562567 |
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complete leydig cell hypoplasia
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C562567 |
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female luteinizing hormone resistance
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C562567 |
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type II leydig cell hypoplasia
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C562567 |
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hypergonadotropic hypogonadism, male, due to LHCGR defect
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C562567 |
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partial leydig cell hypoplasia
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C562567 |
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type i leydig cell hypoplasia
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C562567 |
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luteinizing hormone resistance, female
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C562567 |
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male hypergonadotropic hypogonadism due to LHCGR defect
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C562567 |
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male, due to LHCGR defect hypergonadotropic hypogonadism
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C562567 |
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leydig cell agenesis
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C562567 |
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leydig cell hypoplasia
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C562567 |
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leydig cell hypoplasia with male pseudohermaphroditism
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C562567 |
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leydig cell hypoplasia, complete
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C562567 |
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