{
    "disease_id": "DOID:0111059", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007930", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007930", 
            "name": "Bernard-Soulier syndrome, type A2, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007930", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007930", 
            "name": "BSSA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007930", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007930", 
            "name": "Bernard-Soulier syndrome, type A2, autosomal dominant; BSSA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111059", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111059", 
            "name": "BSSA2"
        }, 
        {
            "url": "https://www.omim.org/entry/153670", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:153670", 
            "name": "Bernard-Soulier syndrome A2, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111059", 
        "description": "A Bernard-Soulier syndrome characterized by autosomal dominant inheritance of mild to moderate bleeding tendency, thrombocytopenia, and an increased mean platelet size that has material_basis_in heterozygous mutations in the GP1BA gene on chromosome 17p.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111059", 
        "name": "Bernard-Soulier syndrome type A2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/153670", 
            "id": "153670", 
            "database": "MIM"
        }
    ]
}