{
    "disease_id": "DOID:0111052", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "Platelet factor X receptor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "SCTS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "familial prothrombin consumption inhibitor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "prothrombin consumption Inhibitor, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "bleeding disorder, Platelet-type, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "prothrombin consumption deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "bleeding abnormality due to deficiency of platelet biding of factor X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "familial prothrombin conversion defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "Scott syndrome; SCTS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "platelet-type bleeding disorder 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "BDPLT7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "prothrombin conversion defect, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009885", 
            "name": "bleeding Abnormality due to deficiency of Platelet binding of Factor 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111052", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111052", 
            "name": "bleeding abnormality due to deficiency of platelet biding of factor X"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111052", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111052", 
            "name": "BDPLT7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111052", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111052", 
            "name": "SCTS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111052", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111052", 
            "name": "familial prothrombin consumption inhibitor"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111052", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111052", 
            "name": "familial prothrombin conversion defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111052", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111052", 
            "name": "platelet-type bleeding disorder 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111052", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111052", 
            "name": "prothrombin consumption deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111052", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111052", 
        "name": "Scott syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111052#disease-associations", 
            "id": "0111052", 
            "database": "Alliance of Genome Resources"
        }
    ]
}