{
    "disease_id": "DOID:0080700", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0080700", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080700", 
            "name": "caudal dysgenesis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080700", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080700", 
            "name": "caudal dysplasia sequence"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080700", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080700", 
            "name": "caudal regression sequence"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080700", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080700", 
            "name": "sacral agenesis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080700", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080700", 
            "name": "sacral defect with anterior meningocele"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080700", 
        "description": "A physical disorder that is characterized by impairment of the development of the lower half of the body.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080700", 
        "name": "caudal regression syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080700#disease-associations", 
            "id": "0080700", 
            "database": "Alliance of Genome Resources"
        }
    ]
}