{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "3MC syndrome caused by mutation in COLEC10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "3MC syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "facial clefting syndrome, Gypsy type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "COLEC10 3MC syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "3MC syndrome 3; 3MC3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "Malpuech Facial clefting syndrome, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "Malpuech Facial clefting syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009554", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009554", 
            "name": "3MC3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060577", 
        "description": "A 3MC syndrome that has_material_basis_in a compound heterozygous mutation in the COLEC10 gene on chromosome 8q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060577", 
        "name": "3MC syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/248340", 
            "id": "248340", 
            "database": "MIM"
        }
    ]
}