{
    "disease_id": "DOID:0110875",
    "recommended_name": {
        "id": "DOID:0110875",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110875",
        "name": "holoprosencephaly 3",
        "description": "A holoprosencephaly that has_material_basis_in heterozygous mutation in the SHH gene on chromosome 7q36."
    },
    "synonyms": [
        {
            "id": "DOID:0110875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110875",
            "name": "HLP3",
            "description": ""
        },
        {
            "id": "DOID:0110875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110875",
            "name": "HPE3",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "holoprosencephaly 3",
            "description": "Any holoprosencephaly in which the cause of the disease is a mutation in the SHH gene."
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "SHH holoprosencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "Shh holoprosencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "HPE3",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "HLP3",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "holoprosencephaly 3",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "holoprosencephaly caused by mutation in Shh",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "holoprosencephaly caused by mutation in SHH",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "holoprosencephaly 3; HPE3",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "Hlp3",
            "description": ""
        },
        {
            "id": "MONDO:0007733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007733",
            "name": "holoprosencephaly type 3",
            "description": ""
        },
        {
            "id": "MIM:142945",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/142945",
            "name": "Holoprosencephaly 3",
            "description": "Holoprosencephaly 3"
        }
    ]
}