{
    "disease_id": "DOID:0111248", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007301", 
            "name": "CCMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007301", 
            "name": "rib Gap defects with micrognathia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007301", 
            "name": "cerebro-costo-mandibular syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007301", 
            "name": "CEREBROCOSTOMANDIBULAR syndrome; CCMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007301", 
            "name": "CCM syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111248", 
            "name": "CCM syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111248", 
            "name": "CCMS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111248", 
            "name": "cerebro-costo-mandibular syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111248", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111248", 
            "name": "rib gap defects with micrognathia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111248", 
        "description": "A syndrome characterized by severe micrognathia, posterior rib and palate defects, and often intellectual disability that has_material_basis_in heterozygous mutation in SNRPB on 20p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111248", 
        "name": "cerebrocostomandibular syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/117650", 
            "id": "117650", 
            "database": "MIM"
        }
    ]
}