{
    "disease_id": "DOID:0060575", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "3MC syndrome caused by mutation in MASP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "3Mc syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "Michels syndrome, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "craniosynostosis with 51D anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "Michels syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "3MC syndrome 1; 3MC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "oculopalatoskeletal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "3MC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "MASP1 3MC syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060575", 
        "description": "A 3MC syndrome that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the mannan binding lectin serine peptidase 1 gene (MASP1) on chromosome 3q27.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060575", 
        "name": "3MC syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/257920", 
            "id": "257920", 
            "database": "MIM"
        }
    ]
}