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F12

coagulation factor XII

gene with protein productOMIM: 6106193 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)2
Congenital factor XII deficiencyORPHA:330
→
F12-associated cold autoinflammatory syndromeORPHA:617919
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Disease-causing germline mutation(s) (gain of function) in1
F12-related hereditary angioedema with normal C1InhORPHA:100054
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Данные: Orphadata (CC-BY-4.0)