Disease table of PROTHROMBIN DEFICIENCY, CONGENITAL OMIM ID: 613679

Gene-disease associations table

Gene	Associated with PROTHROMBIN DEFICIENCY, CONGENITAL in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
F2	ClinVar, OMIM, HUMSAVAR	HGNC link	11p11.2	4	613679, PS188050, 614390, 601367