{
    "disease_id": "DOID:0050885", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013873", 
            "name": "intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013873", 
            "name": "intrauterine growth retardation - metaphyseal dysplasia - adrenal hypoplasia congenita - genital anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013873", 
            "name": "intrauterine growth retardation-metaphyseal dysplasia-adrenal hypoplasia congenita-genital anomalies syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013873", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013873", 
            "name": "intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050885", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050885", 
            "name": "intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050885", 
        "description": "A syndrome that is characterized by intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities and has_material_basis_in heterozygous mutation in the CDKN1C gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050885", 
        "name": "IMAGe syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050885#disease-associations", 
            "id": "0050885", 
            "database": "Alliance of Genome Resources"
        }
    ]
}