{
    "disease_id": "DOID:0110880",
    "recommended_name": {
        "id": "DOID:0110880",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110880",
        "name": "holoprosencephaly 4",
        "description": "A holoprosencephaly that has_material_basis_in heterozygous mutation in the TGIF gene on chromosome 18p11."
    },
    "synonyms": [
        {
            "id": "DOID:0110880",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110880",
            "name": "HPE4",
            "description": ""
        },
        {
            "id": "MONDO:0007734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007734",
            "name": "holoprosencephaly 4",
            "description": "A rare disorder caused by mutations in the TGIF gene mapped to chromosome 18p11.3. It is characterized by semilobar holoprosencephaly, hypotelorism, and ptosis."
        },
        {
            "id": "MONDO:0007734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007734",
            "name": "HPE4",
            "description": ""
        },
        {
            "id": "MONDO:0007734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007734",
            "name": "TGIF1 holoprosencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0007734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007734",
            "name": "holoprosencephaly 4",
            "description": ""
        },
        {
            "id": "MONDO:0007734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007734",
            "name": "holoprosencephaly caused by mutation in TGIF1",
            "description": ""
        },
        {
            "id": "MONDO:0007734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007734",
            "name": "holoprosencephaly type 4",
            "description": ""
        },
        {
            "id": "MIM:142946",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/142946",
            "name": "Holoprosencephaly 4",
            "description": "Holoprosencephaly 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110880"
    ],
    "unlinked_id_list": []
}