{
    "disease_id": "DOID:0111052",
    "recommended_name": {
        "id": "DOID:0111052",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111052",
        "name": "Scott syndrome",
        "description": "A blood coagulation disease characterized by autosomal recessive inheritance of hemorrhagic episodes due to impaired platelet coagulant activity that has material_basis_in homozygous mutation in the TMEM16F gene on chromosome 12q12."
    },
    "synonyms": [
        {
            "id": "DOID:0111052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111052",
            "name": "bleeding abnormality due to deficiency of platelet biding of factor X",
            "description": ""
        },
        {
            "id": "DOID:0111052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111052",
            "name": "BDPLT7",
            "description": ""
        },
        {
            "id": "DOID:0111052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111052",
            "name": "SCTS",
            "description": ""
        },
        {
            "id": "DOID:0111052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111052",
            "name": "familial prothrombin consumption inhibitor",
            "description": ""
        },
        {
            "id": "DOID:0111052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111052",
            "name": "familial prothrombin conversion defect",
            "description": ""
        },
        {
            "id": "DOID:0111052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111052",
            "name": "platelet-type bleeding disorder 7",
            "description": ""
        },
        {
            "id": "DOID:0111052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111052",
            "name": "prothrombin consumption deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "Scott syndrome",
            "description": "Scott syndrome is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity."
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "BDPLT7",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "SCTS",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "Scott syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "bleeding abnormality due to deficiency of platelet biding of factor X",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "familial prothrombin consumption inhibitor",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "familial prothrombin conversion defect",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "platelet-type bleeding disorder 7",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "prothrombin consumption deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "Platelet factor X receptor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "bleeding Abnormality due to deficiency of Platelet binding of Factor 10",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "bleeding disorder, Platelet-type, 7",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "prothrombin consumption inhibitor, familial",
            "description": ""
        },
        {
            "id": "MONDO:0009885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009885",
            "name": "prothrombin conversion defect, familial",
            "description": ""
        },
        {
            "id": "MIM:262890",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/262890",
            "name": "Scott syndrome",
            "description": "Scott syndrome"
        }
    ]
}