Literature summary for 1.6.3.1 extracted from

Bakri, F.G.; Martel, C.; Khuri-Bulos, N.; Mahafzah, A.; El-Khateeb, M.S.; Al-Wahadneh, A.M.; Hayajneh, W.A.; Hamamy, H.A.; Maquet, E.; Molin, M.; Stasia, M.J.
First report of clinical, functional, and molecular investigation of chronic granulomatous disease in nine Jordanian families (2009), J. Clin. Immunol., 29, 215-230.

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Application

Application	Comment	Organism
medicine	chronic granulomatous disease is a rare inherited immunodeficiency syndrome caused by mutations in four genes encoding essential nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex components. Clinical, functional, and molecular investigation of chronic granulomatous disease in nine Jordanian families	Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates	Organism	Comment (Nat. Sub.)	Natural Products	Comment (Nat. Pro.)	Rev.	Reac.
additional information	Homo sapiens	chronic granulomatous disease is a rare inherited immunodeficiency syndrome caused by mutations in four genes encoding essential nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex components	?	-	?

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	-	-	-

Substrates and Products (Substrate)

Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
additional information	chronic granulomatous disease is a rare inherited immunodeficiency syndrome caused by mutations in four genes encoding essential nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex components	Homo sapiens	?	-	?

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Release 2023.1 (January 2023)