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

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000270726 Fertility disorder for over 1.5 years, two miscarriages, one "biochemical" pregnancy. Pregnancy, sinus vein thrombosis, protein C deficiency - 32y Unknown - - - - - Andreas Laner 00375512
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