Details of Disease | DrugMAP

General Information of Disease (ID: DISCYHW2)

Disease Name	Susceptibility to localized juvenile periodontitis
Disease Hierarchy	DIS98MYE: Inherited disease susceptibility DISCYHW2: Susceptibility to localized juvenile periodontitis
Disease Identifiers	MONDO ID MONDO_0018643 UMLS CUI C5681199 MedGen ID 1812489 Orphanet ID 447740 SNOMED CT ID 1197482007

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
FPR1	TT5Y4EM	Supportive	Autosomal recessive	[1]
------------------------------------------------------------------------------------

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
FPR1	OTFF9I6W	Supportive	Autosomal recessive	[1]
------------------------------------------------------------------------------------

References

1	Formylpeptide receptor single nucleotide polymorphism 348T>C and its relationship to polymorphonuclear leukocyte chemotaxis in aggressive periodontitis. J Periodontol. 2009 Sep;80(9):1498-505. doi: 10.1902/jop.2009.090103.