Ontology Browser

Term:
platelet-type bleeding disorder 9 (DOID:0111045)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2)
Parent Terms Term With Siblings Child Terms
Acquired Pure Megakaryocytic Aplasia 
acquired thrombocytopenia +   
Activated Protein C Resistance  
antithrombin III deficiency  
autosomal dominant macrothrombocytopenia TUBB1-related  
Bernard-Soulier syndrome +   
Bleeding Disorder Due To P2rx1 Defect 
Blood Loss, Surgical  
Circumvallate Placenta Syndrome 
congenital afibrinogenemia +   
congenital amegakaryocytic thrombocytopenia  
Congenital Disorder of Glycosylation Type 1X  
DK Phocomelia Syndrome 
Dysprothrombinemia  
Ecchymosis 
Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality 
Epistaxis +   
Essential Athrombia 
Evans' syndrome +   
Exsanguination 
Eye Hemorrhage +   
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  
Forsythe-Wakeling Syndrome 
Gardner Morrisson Abbot Syndrome 
Gastrointestinal Hemorrhage +   
Giant Platelet Syndrome with Thrombocytopenia  
Glanzmann's thrombasthenia +   
gray platelet syndrome +   
hemarthrosis +   
hematocele of tunica vaginalis testis 
Hematoma +   
Hematuria +   
Hemobilia 
Hemoperitoneum 
hemophilia B  
Hemoptysis 
Hemothorax +  
Hermansky-Pudlak syndrome +   
Intracranial Hemorrhages +   
Jacobsen Distal 11q Deletion Syndrome +  
Kasabach-Merritt Syndrome +   
MYH-9 related disease +   
Neonatal Alloimmune Thrombocytopenia  
Oculootoradial Syndrome  
Oral Hemorrhage +  
Passovoy Factor 
Pechet Factor Deficiency 
Phospholipase A2, Group IVA, Deficiency of  
PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE  
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  
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  
An inherited blood coagulation disease characterized by autosomal dominant inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has material_basis_in mutation in the ITGA2 gene on chromosome 5q11.2.
Postoperative Hemorrhage +  
Primary Release Disorder Of Platelets 
Prolonged Bleeding Time, Brachydactyly, and Mental Retardation  
protein C deficiency +   
prothrombin deficiency +   
Pulmonary Hemorrhage +   
purpura +   
qualitative platelet defect 
Quebec platelet disorder  
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia +   
Retrobulbar Hemorrhage 
Rhizomelic Osteochondrodysplasia with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension 
Scott syndrome  
Shock, Hemorrhagic +   
Spastic Paraplegia and Evans Syndrome 
Stormorken syndrome  
Takenouchi-Kosaki Syndrome  
Tetraphocomelia-Thrombocytopenia Syndrome 
thrombocytopenia +   
Thrombocytopenia 1  
Thrombocytopenia 2  
Thrombocytopenia 3  
Thrombocytopenia 4  
THROMBOCYTOPENIA 5  
THROMBOCYTOPENIA 6  
Thrombocytopenia Absent Ulnar Syndrome 
thrombocytopenia due to platelet alloimmunization +   
Thrombocytopenia Robin Sequence 
Thrombocytopenia with Elevated Serum Iga and Renal Disease 
Thrombocytopenia, Anemia, and Myelofibrosis  
Thrombocytopenia, Cyclic 
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis  
thrombocytopenia-absent radius syndrome  
thrombocytosis +   
Thrombotic Microangiopathies +   
transient neonatal thrombocytopenia 
Undefined Platelet Disorder 
Uterine Hemorrhage +   
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  
X-Linked Thrombocytopenia, Intermittent  
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia  

Synonyms
Exact Synonyms: BDPLT9 ;   COLLAGEN PLATELET RECEPTOR DEFICIENCY ;   GP IA Deficiency ;   Glycoprotein IA Deficiency
Primary IDs: MESH:C566000
Alternate IDs: OMIM:614200 ;   RDO:0014486
Xrefs: ORDO:98886
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/2933589, https://www.ncbi.nlm.nih.gov/pubmed/2943331

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.