{
    "disease_id": "DOID:2219", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "platelet-type bleeding disorder 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "platelet glycoprotein IIb-IIIa deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "Glycoprotein IIb/IIIa defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "Thrombocytasthenia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "deficiency of GP IIb-IIIa complex"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "BDPLT2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "thrombasthenia of Glanzmann and Naegeli"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "deficiency of glycoprotein complex IIb-IIIa"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "Glanzmann thrombasthenia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2219", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2219", 
            "name": "deficiency of platelet fibrinogen receptor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "Glanzmann thrombasthenia (GT) is a bleeding syndrome characterized by spontaneous mucocutaneous bleeding and an exaggerated response to trauma due to a constitutional thrombocytopenia.", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Glanzmann's thrombasthenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "thrombasthenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Thrombocytasthenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "BDPLT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "deficiency of GP 2B 3A complex"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "glycoprotein Complex IIb-IIIa, deficiency of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Diacyclothrombopathia 2B 3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "thrombasthenia of Glanzmann and Naegeli"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "deficiency of glycoprotein complex IIb-IIIa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "deficiency of platelet fibrinogen receptor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "GT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Glanzmann thrombasthenia; GT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Platelet glycoprotein IIb-IIIa deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "platelet-type bleeding disorder 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Glanzmann thrombasthenia type A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Platelet fibrinogen receptor, deficiency of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "GP IIb-IIIa Complex, deficiency of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "platelet glycoprotein IIb-IIIa deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "glycoprotein IIb/IIIa defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "deficiency of GP IIb-IIIa complex"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "bleeding disorder, Platelet-type, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Platelet glycoprotein 2B 3A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010119", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010119", 
            "name": "Glanzmann thrombasthenia"
        }, 
        {
            "url": "https://www.omim.org/entry/273800", 
            "description": "Glanzmann thrombasthenia", 
            "resource": "MIM", 
            "id": "MIM:273800", 
            "name": "Glanzmann thrombasthenia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2219", 
        "description": "A blood coagulation disease characterized by autosomal recessive inheritance of failure of platelet aggregation and absent or diminished clot retraction that has material_basis_in mutation in the ITGA2B or ITGB3 genes on chromosome 17q21.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2219", 
        "name": "Glanzmann's thrombasthenia"
    }
}