{
    "disease_id": "DOID:0111675",
    "recommended_name": {
        "id": "DOID:0111675",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111675",
        "name": "neurooculocardiogenitourinary syndrome",
        "description": "A syndrome characterized by impaired growth and anomalies of the ocular, craniofacial, neurologic, cardiovascular, genitourinary, skeletal, and gastrointestinal systems that has_material_basis_in heterozygous mutation in WDR37 on chromosome 10p15.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111675",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111675",
            "name": "NOCGUS",
            "description": ""
        },
        {
            "id": "MIM:618652",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618652",
            "name": "Neurooculocardiogenitourinary syndrome",
            "description": "Neurooculocardiogenitourinary syndrome"
        }
    ]
}