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
hypertyrosinemias, type i D020176
richner hanhart syndrome D020176
hereditary tyrosinemia D020176
hereditary tyrosinemia, type II D020176
hereditary tyrosinemia, type III D020176
hereditary tyrosinemia, type i D020176
hereditary tyrosinemias D020176
oculocutaneous type tyrosinoses D020176
oculocutaneous type tyrosinosis D020176
oregon type tyrosinemia D020176
richner-hanhart syndrome D020176
richner-hanhart syndrome, tyrosinosis, oculocutaneous type D020176
richner-hanhart syndromes D020176
type i hereditary tyrosinemia D020176
syndrome, richner-hanhart D020176