Disease #01582 (THPH2 (thrombophilia, due to activated protein C resistance (THPH2)), OMIM:188055)

Official abbreviation THPH2
Name thrombophilia, due to activated protein C resistance (THPH2)
OMIM ID 188055
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene F5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2019-12-02 15:51:36 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00024937 - PubMed: Bertina 1994, Journal: Bertina 1994 4-generation family, 13 affecteds (4F, 9M) - - Netherlands - - - - - THPH2 n-APC-SR <0.84 (mean 0.65, range 0.59-0.71) F5 F5 1 13 Johan den Dunnen
00024938 - PubMed: Bertina 1994, Journal: Bertina 1994 64 APC resistant patients of 301 with first episode deep vein thrombosis - no Netherlands - - - - - THPH2 n-APC-SR <0.84 F5 F5 2 64 Johan den Dunnen
00165498 11372696-Pat? PubMed: Wylenzek 2001 - - - - - - - - - THPH2 - F2 F2 1 1 Johan den Dunnen
00165582 14617013-Pat? PubMed: Mumford 2003 - - - - - - - - - THPH2 - F5 F5 1 1 Johan den Dunnen
00165674 9454741-Pat? PubMed: Chan 1998 - - - - - - - - - THPH2 - F5 F5 1 1 Johan den Dunnen
00165675 9454742-Pat? PubMed: Williamson 1998 - - - - - - - - - THPH2 - F5 F5 1 1 Johan den Dunnen
00165677 9694743-Pat? PubMed: Lunghi 1998 - - - - - - - - - THPH2 - F5 F5 1 1 Johan den Dunnen
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