Details of Disease | DrugMAP

General Information of Disease (ID: DISNNKF2)

Disease Name	Obsolete hereditary pediatric Behet-like disease
Disease Hierarchy	DIS01GPL: Grass pollen hypersensitivity DISNNKF2: Obsolete hereditary pediatric Behet-like disease

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
TNFAIP3	TT5W0IO	Moderate	Autosomal dominant	[1]
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This Disease Is Related to 2 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
RELA	OTUJP9CN	Supportive	Autosomal dominant	[2]
TNFAIP3	OTVLI4DD	Moderate	Autosomal dominant	[1]
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References

1	Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.
2	A Novel RELA Truncating Mutation in a Familial Beh?et's Disease-like Mucocutaneous Ulcerative Condition. Arthritis Rheumatol. 2021 Mar;73(3):490-497. doi: 10.1002/art.41531. Epub 2021 Feb 15.