Phenotypes for disease #00457 (afibrinogenemia, congenital, OMIM:202400)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000016245 hypofibrinogenemiano history of thrombosis or hemorrhage - - Familial - - - - - Johan den Dunnen 00017892
0000016246 see paper; dysfibrinogenemia, abnormally prolonged thrombin time - - Familial 48y - - - - Johan den Dunnen 00017893
0000016247 see paper - - Familial - - - - - Johan den Dunnen 00017894
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