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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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kallmann syndrome
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D017436 |
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kallmann syndrome 1
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D017436 |
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kallmann syndrome 2
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D017436 |
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kallmann syndrome 3
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D017436 |
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kallmann syndrome, type 1, X-linked
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D017436 |
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kallmann syndrome, type 3, recessive
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D017436 |
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kallmanns syndrome
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D017436 |
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Kallmann's syndrome
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D017436 |
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anosmia, and midline cranial anomalies (cleft lip, cleft palate and imperfect fusion) hypogonadotropic hypogonadism
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D017436 |
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anosmic hypogonadism
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D017436 |
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anosmic hypogonadisms
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D017436 |
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anosmic idiopathic hypogonadotropic hypogonadism
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D017436 |
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autosomal dominant form of kallmann syndrome
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D017436 |
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autosomal recessive form of kallmann syndrome
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D017436 |
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dysplasia olfactogenitalis of de morsier
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D017436 |
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