{
    "disease_id": "DOID:0060242", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "synpolydactyly type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "HOXD13 non-syndromic synpolydactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "SPD, Vordingborg type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "synpolydactyly, Vordingborg type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "SPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "synpolydactyly 1; SPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "non-syndromic synpolydactyly caused by mutation in HOXD13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "SD2, Vordingborg type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "syndactyly, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "synpolydactyly 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "synpolydactyly with foot anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008513", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008513", 
            "name": "SD2a"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060242", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060242", 
            "name": "syndactyly type 2"
        }, 
        {
            "url": "https://www.omim.org/entry/186000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:186000", 
            "name": "Synpolydactyly 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060242", 
        "description": "A syndactyly characterized by an increased number of digits; often a result of a mutation in the HOXD13 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060242", 
        "name": "synpolydactyly"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/186000", 
            "id": "186000", 
            "database": "MIM"
        }
    ]
}