General Information of Disease (ID: DIS2I6LU)

Disease Name Autosomal recessive extra-oral halitosis
Disease Hierarchy
DISCPWH9: Autosomal recessive disease
DISUP794: Inborn disorder of methionine cycle and sulfur amino acid metabolism
DIS2I6LU: Autosomal recessive extra-oral halitosis

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
SELENBP1 OT3NZNTR Supportive Autosomal recessive [1]
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References

1 Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis. Nat Genet. 2018 Jan;50(1):120-129. doi: 10.1038/s41588-017-0006-7. Epub 2017 Dec 18.