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platelet-type bleeding disorder 14 (DOID:0111047)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
acquired von Willebrand syndrome 
Activated Protein C Resistance  
antithrombin III deficiency  
Bernard-Soulier syndrome +   
Bleeding Disorder, East Texas Type 
Car Factor Deficiency 
coagulation protein disease +   
congenital afibrinogenemia +   
disseminated intravascular coagulation +   
Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality 
Essential Athrombia 
essential thrombocythemia  
factor V deficiency +   
factor VII deficiency  
factor VIII deficiency +   
factor X deficiency  
factor XI deficiency  
factor XII deficiency  
factor XIII deficiency +   
Factors VIII, IX and XI, Combined Deficiency of 
Familial Multiple Coagulation Factor Deficiency II 
Familial Multiple Coagulation Factor Deficiency IV 
Familial Multiple Coagulation Factor Deficiency VI 
Familial Platelet Disorder with Associated Myeloid Malignancy  
Fibrinolytic Defect 
Flaujeac Factor Deficiency  
Glanzmann's thrombasthenia +   
Globulin Anomaly involving Beta (2A)-Globulin 
gray platelet syndrome +   
hemophilia B  
hemorrhagic disease +   
Hermansky-Pudlak syndrome +   
inherited blood coagulation disease +   
MYH-9 related disease +   
Passovoy Factor 
Pechet Factor Deficiency 
Phospholipase A2, Group IVA, Deficiency of  
Plasma Clot Retraction Factor, Deficiency of 
Platelet Aggregation, Spontaneous 
Platelet Factor 3 Deficiency 
Platelet Prostacyclin Receptor Defect 
Platelet Receptor for Collagen, Deficiency of 
Platelet Signal Processing Defect 
platelet storage pool deficiency +   
platelet-type bleeding disorder 10  
platelet-type bleeding disorder 11  
platelet-type bleeding disorder 12 
Platelet-Type Bleeding Disorder 13  
platelet-type bleeding disorder 14  
An inherited blood coagulation disease characterized by autosomal dominant inheritance of defective platelet aggegation, epistaxis, ecchymoses, and prolonged bleeding times that has material basis in mutation in the TBXAS1 gene on chromosome 7q34. (DO)
platelet-type bleeding disorder 15  
platelet-type bleeding disorder 16  
platelet-type bleeding disorder 17  
platelet-type bleeding disorder 18  
platelet-type bleeding disorder 19  
platelet-type bleeding disorder 20  
Platelet-Type Bleeding Disorder 21  
platelet-type bleeding disorder 3  
platelet-type bleeding disorder 8  
platelet-type bleeding disorder 9  
Prekallikrein Deficiency  
Primary Release Disorder Of Platelets 
Prolonged Bleeding Time, Brachydactyly, and Mental Retardation  
protein C deficiency +   
protein S deficiency +   
prothrombin deficiency +   
purpura +   
qualitative platelet defect 
Quebec platelet disorder  
Scott syndrome  
Stormorken syndrome  
thrombocytopenia +   
thrombocytosis +   
thrombophilia +   
Undefined Platelet Disorder 
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1  
Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2  
von Willebrand's disease +   
White Platelet Syndrome 
Wiskott-Aldrich syndrome +   
X-Linked Anemia with or without Neutropenia and/or Platelet Abnormalities  

Exact Synonyms: BDPLT14 ;   thromboxane synthase deficiency
Primary IDs: MESH:C562866 ;   RDO:0012401
Alternate IDs: OMIM:614158
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/6268139

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