PubDictionaries

manager	yucca
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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

There is 0 pattern entry.

Label	Id

CGD, autosomal recessive cytochrome b-positive, type i	C565532
autosomal recessive cytochrome b-positive, type i CGD	C565532
chronic, autosomal recessive, cytochrome b-positive, type i granulomatous disease	C565532
chronic, due to NCF1 deficiency granulomatous disease	C565532
deficiency of neutrophil cytosol factor 1	C565532
deficiency of p47-phox	C565532
deficiency of soluble oxidase component II	C565532
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i	C565532
granulomatous disease, chronic, due to NCF1 deficiency	C565532
neutrophil cytosol factor 1, deficiency of	C565532
p47-phox, deficiency of	C565532
soluble oxidase component II, deficiency of	C565532