{
    "disease_id": "DOID:14766", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:14766", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14766", 
            "name": "hereditary renal aplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14766", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14766", 
            "name": "hereditary urogenital adysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14766", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14766", 
            "name": "renal adysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14766", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14766", 
            "name": "renal aplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/191830", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:191830", 
            "name": "Renal hypodysplasia/aplasia 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14766", 
        "description": "A renal disease that is characterized by the failure of one or both kidneys to develop.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14766", 
        "name": "renal agenesis"
    }
}