{
    "disease_id": "DOID:0111675", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111675", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111675", 
            "name": "NOCGUS"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111675", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111675", 
        "name": "neurooculocardiogenitourinary syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618652", 
            "id": "618652", 
            "database": "MIM"
        }
    ]
}