{
    "disease_id": "DOID:0070684",
    "recommended_name": {
        "id": "DOID:0070684",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070684",
        "name": "congenital hydrocephalus 3",
        "description": "A congenital hydrocephalus that has_material_basis_in homozygous mutation in the WDR81 gene on chromosome 17p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0054794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054794",
            "name": "hydrocephalus, congenital, 3, with brain anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0054794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054794",
            "name": "HYC3",
            "description": ""
        },
        {
            "id": "MONDO:0054794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054794",
            "name": "hydrocephalus, nonsyndromic, autosomal recessive 3",
            "description": ""
        },
        {
            "id": "MIM:617967",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617967",
            "name": "Hydrocephalus, congenital, 3, with brain anomalies",
            "description": "Hydrocephalus, congenital, 3, with brain anomalies"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070684"
    ],
    "unlinked_id_list": []
}