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).

There is 0 pattern entry.

Label	Id

GSD9B	C563008
GSD IXB	C563008
autosomal recessive glycogenosis of liver and muscle	C563008
autosomal recessive phosphorylase kinase deficiency of liver and muscle	C563008
glycogen storage disease IXB	C563008
glycogenosis of liver and muscle, autosomal recessive	C563008
phosphorylase kinase deficiency of liver and muscle, autosomal recessive	C563008