{
    "disease_id": "DOID:0060327", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008124", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008124", 
            "name": "omphalocele, autosomal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008124", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008124", 
            "name": "type - hypogastric - defect in the caudal fold"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008124", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008124", 
            "name": "type - epigastric - defect in the cephalic fold"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008124", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008124", 
            "name": "chromosome 1P31 Duplication syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008124", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008124", 
            "name": "paraomphalocele"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060327", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060327", 
            "name": "omphalocoele"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060327", 
        "description": "A physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060327", 
        "name": "omphalocele"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060327#disease-associations", 
            "id": "0060327", 
            "database": "Alliance of Genome Resources"
        }
    ]
}