{
    "disease_id": "DOID:0110878",
    "recommended_name": {
        "id": "DOID:0110878",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110878",
        "name": "holoprosencephaly 5",
        "description": "A holoprosencephaly that has_material_basis_in heterozygous mutation in the ZIC2 gene on chromosome 13q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110878",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110878",
            "name": "HPE5",
            "description": ""
        },
        {
            "id": "MONDO:0012322",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012322",
            "name": "holoprosencephaly 5",
            "description": "Holoprosencephaly associated with mutations in the ZIC2 gene."
        },
        {
            "id": "MONDO:0012322",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012322",
            "name": "HPE5",
            "description": ""
        },
        {
            "id": "MONDO:0012322",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012322",
            "name": "ZIC2 holoprosencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0012322",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012322",
            "name": "holoprosencephaly 5",
            "description": ""
        },
        {
            "id": "MONDO:0012322",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012322",
            "name": "holoprosencephaly caused by mutation in ZIC2",
            "description": ""
        },
        {
            "id": "MONDO:0012322",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012322",
            "name": "holoprosencephaly type 5",
            "description": ""
        },
        {
            "id": "MIM:609637",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609637",
            "name": "Holoprosencephaly 5",
            "description": "Holoprosencephaly 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110878"
    ],
    "unlinked_id_list": []
}