{
    "disease_id": "DOID:14679", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008642", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008642", 
            "name": "VACTERL/vater association"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008642", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008642", 
            "name": "VATER/VACTERL association"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008642", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008642", 
            "name": "vertebral abnormalities, anal atresia, Cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008642", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008642", 
            "name": "VATER syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008642", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008642", 
            "name": "VATER association"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14679", 
        "description": "A syndrome that is characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14679", 
        "name": "VACTERL association"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14679#disease-associations", 
            "id": "14679", 
            "database": "Alliance of Genome Resources"
        }
    ]
}