{
    "disease_id": "DOID:0110975", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012658", 
            "name": "BDB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012658", 
            "name": "brachydactyly, type B2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012658", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012658", 
            "name": "brachydactyly, type B2; BDB2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110975", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110975", 
            "name": "BDB2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110975", 
        "description": "A brachydactyly characterized by hypoplasia/aplasia of distal phalanges, distal symphalangism, fusion of carpal/tarsal bones, and partial cutaneous syndactyly that has_material_basis_in mutations in the NOG gene on chromosome 17q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110975", 
        "name": "brachydactyly type B2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110975#disease-associations", 
            "id": "0110975", 
            "database": "Alliance of Genome Resources"
        }
    ]
}