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
hyperphenylalaninemia, non phenylketonuric D010661
hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to DHPR deficiency D010661
non phenylketonuric hyperphenylalaninemia D010661
non-phenylketonuric hyperphenylalaninemia D010661
non-phenylketonuric hyperphenylalaninemias D010661
tetrahydrobiopterin deficiency D010661
phenylalanine hydroxylase deficiency D010661
phenylalanine hydroxylase deficiency disease D010661
phenylalanine hydroxylase deficiency disease, severe D010661
phenylalanine hydroxylase, severe deficiency disease D010661
phenylketonuria D010661
phenylketonuria II D010661
phenylketonuria i D010661
phenylketonuria type 2 D010661
phenylketonuria, atypical D010661