PubDictionaries

"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease.tsv"
"Addition_for_LitCoin_Disease_2.tsv"

There is 0 pattern entry.

Label	Id

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