Disease #01581 (THPH1 (thrombophilia,due to thrombin defect (THPH1)), OMIM:188050)

Official abbreviation THPH1
Name thrombophilia,due to thrombin defect (THPH1)
OMIM ID 188050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 4 genes F13A1, F2, HABP2, MTHFR
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Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00155217 - - - - - - - - 0 - - THPH1 - PROS1 PROS1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00165501 12218454-Pat? PubMed: Warshawsky 2002 - - - - - - 0 - - THPH1 - F2 F2 1 1 Johan den Dunnen
00165519 17461935-Pat? PubMed: Flaujac 2007 - - - - - - 0 - - THPH1 - F2 F2 1 1 Johan den Dunnen
00165529 8916933-Pat? PubMed: Poort 1996 - - - - - - 0 - - THPH1 - F2 F2 1 1 Johan den Dunnen
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