{
    "disease_id": "DOID:0070685",
    "recommended_name": {
        "id": "DOID:0070685",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070685",
        "name": "congenital hydrocephalus 4",
        "description": "A congenital hydrocephalus that has_material_basis_in heterozygous mutation in the TRIM71 gene on chromosome 3p22."
    },
    "synonyms": [
        {
            "id": "MONDO:0032862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032862",
            "name": "hydrocephalus, congenital communicating, 1",
            "description": ""
        },
        {
            "id": "MONDO:0032862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032862",
            "name": "HYDCC1",
            "description": ""
        },
        {
            "id": "MIM:618667",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618667",
            "name": "Hydrocephalus, congenital, 4",
            "description": "Hydrocephalus, congenital, 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070685"
    ],
    "unlinked_id_list": []
}