{
    "disease_id": "DOID:2219",
    "recommended_name": {
        "id": "DOID:2219",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2219",
        "name": "Glanzmann's thrombasthenia",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "BDPLT2",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "Glanzmann thrombasthenia",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "Glycoprotein IIb/IIIa defect",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "Thrombocytasthenia",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "deficiency of GP IIb-IIIa complex",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "deficiency of glycoprotein complex IIb-IIIa",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "deficiency of platelet fibrinogen receptor",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "platelet glycoprotein IIb-IIIa deficiency",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "platelet-type bleeding disorder 2",
            "description": ""
        },
        {
            "id": "DOID:2219",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2219",
            "name": "thrombasthenia of Glanzmann and Naegeli",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Glanzmann's thrombasthenia",
            "description": "Glanzmann thrombasthenia (GT) is a bleeding syndrome characterized by spontaneous mucocutaneous bleeding and an exaggerated response to trauma due to a constitutional thrombocytopenia."
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "deficiency of GP IIb-IIIa complex",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Glanzmann thrombasthenia; GT",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Platelet fibrinogen receptor, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Glanzmann thrombasthenia",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "thrombasthenia",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "GP IIb-IIIa Complex, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "platelet glycoprotein IIb-IIIa deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Diacyclothrombopathia 2B 3A",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Thrombocytasthenia",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "glycoprotein Complex IIb-IIIa, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Platelet glycoprotein 2B 3A deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "glycoprotein IIb/IIIa defect",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "deficiency of glycoprotein complex IIb-IIIa",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "bleeding disorder, Platelet-type, 2",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "GT",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "platelet-type bleeding disorder 2",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Glanzmann thrombasthenia type A",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "BDPLT2",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "deficiency of GP 2B 3A complex",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "deficiency of platelet fibrinogen receptor",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "thrombasthenia of Glanzmann and Naegeli",
            "description": ""
        },
        {
            "id": "MONDO:0010119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010119",
            "name": "Platelet glycoprotein IIb-IIIa deficiency",
            "description": ""
        },
        {
            "id": "MIM:273800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/273800",
            "name": "Glanzmann thrombasthenia 1",
            "description": "Glanzmann thrombasthenia 1"
        }
    ]
}