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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
alpha granule disease +  
alpha-2-plasmin inhibitor deficiency 
anti-GAD65 autoimmune neurological syndromes  
anti-neutrophil antibody associated vasculitis  
antiphospholipid syndrome  
autoimmune bullous skin disease +   
Autoimmune Hepatitis  
autoimmune thrombocytopenic purpura 
An autoimmune disorder in which the number of circulating platelets is reduced due to their antibody-mediated destruction. ITP is a diagnosis of exclusion and is heterogeneous in origin.
autoimmune thyroid disease +   
autosomal dominant macrothrombocytopenia +  
Behcet's syndrome  
Bernard-Soulier syndrome 
bleeding diathesis due to thromboxane synthesis deficiency 
bleeding disorder, platelet-type, 24 
CNS demyelinating autoimmune disease +   
congenital amegakaryocytic thrombocytopenia +  
congenital factor V deficiency 
congenital factor XI deficiency 
congenital factor XII deficiency 
congenital high-molecular-weight kininogen deficiency 
congenital plasminogen activator inhibitor type 1 deficiency 
congenital thrombotic thrombocytopenic purpura 
congenital vitamin K-dependent coagulation factors deficiency +  
cryoglobulinemia  
cutaneous lupus erythematosus +   
cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder 
Ehlers-Danlos syndrome, fibronectinemic type 
Eosinophilia-Myalgia Syndrome 
Evans syndrome 
factor V and factor VIII, combined deficiency of, type 1 
factor XIII, A subunit, deficiency of 
familial thrombomodulin anomalies 
Glanzmann thrombasthenia +  
Granulomatosis with Polyangiitis +   
gray platelet syndrome 
Guillain-Barre syndrome +  
hemophilia A +  
hemophilia B +  
hereditary hemolytic uremic syndrome +  
hereditary thrombocytopenia and hematologic cancer predisposition syndrome +  
hereditary thrombocytosis with transverse limb defect 
hereditary von Willebrand disease +  
Hermansky-Pudlak syndrome +  
hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 
hypoplasminogenemia 
inflammatory bowel disease +   
inherited prekallikrein deficiency 
inherited thrombophilia +  
isolated delta-storage pool disease 
juvenile idiopathic arthritis +   
latent autoimmune diabetes in adults  
macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 
macrothrombocytopenia, isolated +  
malacoplakia 
monogenic diabetes +  
Myasthenia gravis +   
oroficial granulomatosis 
platelet-type bleeding disorder 10 
platelet-type bleeding disorder 11 
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 8 
platelet-type bleeding disorder 9 
platelet-type von Willebrand disease 
Quebec platelet disorder 
reactive arthritis 
rheumatoid arthritis +   
Scott syndrome 
Sjogren syndrome  
STAT3 gain of function 
Susac Syndrome 
syndromic constitutional thrombocytopenia +  
systemic lupus erythematosus +   
thrombocytopenia 1 
thrombocytopenia 12 with or without myopathy 
thrombocytopenia 2 
thrombocytopenia 3 
thrombocytopenia 4  
thrombocytopenia 5 
thrombocytopenia 7 
thrombocytopenia, X-linked, with or without dyserythropoietic anemia +  
thrombotic thrombocytopenic purpura +  
Vitiligo  
Wiskott-Aldrich syndrome 

Synonyms
Exact Synonyms: ITP ;   Immune thrombocytopenic purpura (disorder) ;   idiopathic thrombocytopenia ;   idiopathic thrombocytopenia purpura ;   idiopathic thrombocytopenic purpura ;   immune thrombocytopenia ;   primary thrombocytopenic purpura
Related Synonyms: AITP ;   Ideopath thrombocytopenic pur ;   idiopathic purpura ;   immune thrombocytopenic purpura ;   werlhof's disease
Xrefs: DOID:8924 ;   GARD:5194 ;   ICD9:287.31 ;   MEDGEN:584986 ;   MIM:188030 ;   MONDO:0008558 ;   MeSH:D016553 ;   MedDRA:10021245 ;   MedDRA:10083842 ;   NANDO:1200315
External Ontologys: disease_has_location EFO:CL:0000233 ;   has_disease_location EFO:CL:0000233
Definition Sources: NCIT:P378

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