Hereditary angioedema

F12 - hereditary angioedema type 3 (FXII)

This test is available for the following conditions:

• Conditions > Hematological, hereditary > Hereditary angioedema

This product is also part of the following panels:

• Comprehensive preconception carrier test panel¹
• Hemostatic/thrombotic disorders panel
• Mendelian inherited disorders panel with genome wide CNV analysis
• Primary immunodeficiencies panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

• Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 610618
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

---