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