{
    "disease_id": "DOID:0110969", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007220", 
            "name": "ROR2 brachydactyly type B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007220", 
            "name": "brachydactyly type B caused by mutation in ROR2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007220", 
            "name": "BDB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007220", 
            "name": "brachydactyly, type B1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007220", 
            "name": "brachydactyly, type B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007220", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007220", 
            "name": "brachydactyly, type B1; BDB1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110969", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110969", 
            "name": "BDB1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110969", 
        "description": "A brachydactyly characterized by short middle phalanges, rudimentary or absent terminal phalanges and nail aplasia that has_material_basis_in heterozygous mutation in the ROR2 gene on chromosome 9q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110969", 
        "name": "brachydactyly type B1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110969#disease-associations", 
            "id": "0110969", 
            "database": "Alliance of Genome Resources"
        }
    ]
}