{
    "disease_id": "DOID:0060225", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009770", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009770", 
            "name": "3MC syndrome 1"
        }, 
        {
            "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"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060225", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060225", 
            "name": "craniofacial-ulnar-renal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060225", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060225", 
            "name": "oculopalatoskeletal syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/257920", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:257920", 
            "name": "3MC syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060225", 
        "description": "A syndrome characterized by blepharophimosis, blepharoptosis, highly arched eyebrows hypertelorism, cleft lip and palate, postnatal growth deficiency, cognitive impairment, hearing loss and, in a smaller percentage of cases, craniosynostosis, radioulnar synostosis and genital and vesicorenal anomalies. It encompasses four disorders that were previously designated the Malpuech, Michels, Mingarelli and Carnevale syndromes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060225", 
        "name": "3MC syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/257920", 
            "id": "257920", 
            "database": "MIM"
        }
    ]
}