Disease #02660 (VKCFD2 (vitamin K-dependent clotting factors, combined deficiency of, type 2 (VKCFD-2)), OMIM:607473)

Official abbreviation VKCFD2
Name vitamin K-dependent clotting factors, combined deficiency of, type 2 (VKCFD-2)
OMIM ID 607473
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene VKORC1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00022457 - PubMed: Rost 2004 4-generation family, 5 affecteds (4F, M), unaffected carruer parents - yes Lebanon - - - - - VKCFD2 see paper VKORC1 VKORC1 1 5 Johan den Dunnen
00022458 - PubMed: Rost 2004 2-generation family, 2 affecteds (2F), unaffected carrier parents F ? Germany - - - - - VKCFD2 see paper VKORC1 VKORC1 1 2 Johan den Dunnen
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