{
    "disease_id": "DOID:0110872",
    "recommended_name": {
        "id": "DOID:0110872",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110872",
        "name": "holoprosencephaly 2",
        "description": "A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21."
    },
    "synonyms": [
        {
            "id": "DOID:0110872",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110872",
            "name": "HPE2",
            "description": ""
        },
        {
            "id": "MONDO:0007999",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007999",
            "name": "holoprosencephaly 2",
            "description": "A rare disorder characterized by the partial separation of the cerebral hemispheres. It is associated with mutations in the SIX3 gene."
        },
        {
            "id": "MONDO:0007999",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007999",
            "name": "holoprosencephaly caused by mutation in SIX3",
            "description": ""
        },
        {
            "id": "MONDO:0007999",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007999",
            "name": "holoprosencephaly 2",
            "description": ""
        },
        {
            "id": "MONDO:0007999",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007999",
            "name": "SIX3 holoprosencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0007999",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007999",
            "name": "holoprosencephaly type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007999",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007999",
            "name": "holoprosencephaly 2; HPE2",
            "description": ""
        },
        {
            "id": "MONDO:0007999",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007999",
            "name": "HPE2",
            "description": ""
        },
        {
            "id": "MIM:157170",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/157170",
            "name": "Holoprosencephaly 2",
            "description": "Holoprosencephaly 2"
        }
    ]
}