Disease #01525 (THPH3 (thrombophilia, hereditary, due to protein C deficiency, autosomal dominant (THPH3)), OMIM:176860)

Official abbreviation THPH3
Name thrombophilia, hereditary, due to protein C deficiency, autosomal dominant (THPH3)
OMIM ID 176860
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PROC
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2019-12-02 15:49:14 +01:00 (CET)


Individuals

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00375512 179584 - - F ? Germany - - - - - THPH3 Fertility disorder for over 1.5 years, two miscarriages, one "biochemical" pregnancy. Pregnancy, sinus vein thrombosis, protein C deficiency PROC PROC 1 1 Andreas Laner
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