{
    "disease_id": "DOID:0110873",
    "recommended_name": {
        "id": "DOID:0110873",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110873",
        "name": "holoprosencephaly 9",
        "description": "A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14."
    },
    "synonyms": [
        {
            "id": "DOID:0110873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110873",
            "name": "pituitary anomalies with holoprosencephaly-like features",
            "description": ""
        },
        {
            "id": "DOID:0110873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110873",
            "name": "HPE9",
            "description": ""
        },
        {
            "id": "DOID:0110873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110873",
            "name": "holoprosencephaly with microphthalmia and first branchial arch anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "holoprosencephaly 9",
            "description": "Any holoprosencephaly in which the cause of the disease is a mutation in the GLI2 gene."
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "GLI2 holoprosencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "HPE9",
            "description": ""
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "holoprosencephaly 9",
            "description": ""
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "holoprosencephaly caused by mutation in GLI2",
            "description": ""
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "holoprosencephaly type 9",
            "description": ""
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "holoprosencephaly with microphthalmia and first branchial arch anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0012563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012563",
            "name": "pituitary anomalies with holoprosencephaly-like features",
            "description": ""
        },
        {
            "id": "MIM:610829",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610829",
            "name": "Holoprosencephaly 9",
            "description": "Holoprosencephaly 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110873"
    ],
    "unlinked_id_list": []
}