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Ontology Browser

Term:
Familial Multiple Coagulation Factor Deficiency II (DOID:9002866)
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Parent Terms Term With Siblings Child Terms
antithrombin III deficiency  
Bernard-Soulier syndrome +   
congenital afibrinogenemia +   
Dysprothrombinemia 
Essential Athrombia 
factor V deficiency +   
factor VII deficiency  
factor VIII deficiency +   
factor X deficiency  
factor XI deficiency  
factor XII deficiency  
factor XIII deficiency +   
Familial Multiple Coagulation Factor Deficiency II 
Familial Multiple Coagulation Factor Deficiency IV 
Familial Multiple Coagulation Factor Deficiency V 
Familial Multiple Coagulation Factor Deficiency VI 
Familial Platelet Disorder with Associated Myeloid Malignancy  
Glanzmann's thrombasthenia +   
gray platelet syndrome +   
hemophilia B  
hereditary combined deficiency of vitamin K-dependent clotting factors +   
Hermansky-Pudlak syndrome +   
high molecular weight kininogen deficiency  
Passovoy Factor 
Pechet Factor Deficiency 
platelet-type bleeding disorder 10  
platelet-type bleeding disorder 11  
platelet-type bleeding disorder 12 
platelet-type bleeding disorder 14  
platelet-type bleeding disorder 15  
platelet-type bleeding disorder 17  
platelet-type bleeding disorder 18  
platelet-type bleeding disorder 19  
platelet-type bleeding disorder 20  
platelet-type bleeding disorder 3  
platelet-type bleeding disorder 8  
platelet-type bleeding disorder 9  
Prolonged Bleeding Time, Brachydactyly, and Mental Retardation 
protein C deficiency +   
prothrombin deficiency +   
Scott syndrome  
thrombophilia due to activated protein C resistance  
von Willebrand's disease +   
Wiskott-Aldrich syndrome +   

Synonyms
Exact Synonyms: F8F9D ;   FMFD II ;   Factor VIII And Factor IX, Combined Deficiency
Primary IDs: MESH:C565024
Alternate IDs: MIM:134510

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