{
    "disease_id": "DOID:0111712",
    "recommended_name": {
        "id": "DOID:0111712",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111712",
        "name": "Kagami-Ogata syndrome",
        "description": "A syndrome characterized by polyhydramnios, fetal macrosomia, abdominal wall defects, skeletal abnormalities, feeding difficulties and impaired swallowing, dysmorphic features, developmental delay and intellectual disability that has_material_basis_in heterozygous mutation in an imprinting region on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "DOID:0111712",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111712",
            "name": "KOS",
            "description": ""
        },
        {
            "id": "MONDO:0011975",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011975",
            "name": "paternal uniparental disomy of chromosome 14",
            "description": ""
        },
        {
            "id": "MONDO:0011975",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011975",
            "name": "paternal uniparental disomy of chromosome type 14",
            "description": ""
        },
        {
            "id": "MONDO:0011975",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011975",
            "name": "UPD(14)pat",
            "description": ""
        },
        {
            "id": "MONDO:0011975",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011975",
            "name": "KAGAMI-Ogata syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011975",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011975",
            "name": "paternal uniparental disomy 14",
            "description": ""
        },
        {
            "id": "MONDO:0011975",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011975",
            "name": "uniparental disomy, paternal, chromosome 14",
            "description": ""
        }
    ]
}