{
    "disease_id": "DOID:0060225",
    "recommended_name": {
        "id": "DOID:0060225",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060225",
        "name": "3MC syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060225",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060225",
            "name": "craniofacial-ulnar-renal syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060225",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060225",
            "name": "oculopalatoskeletal syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "3MC syndrome 1",
            "description": "Any 3MC syndrome in which the cause of the disease is a mutation in the MASP1 gene."
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "3MC syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "3MC syndrome caused by mutation in MASP1",
            "description": ""
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "3MC syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "3Mc syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "MASP1 3MC syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "3MC1",
            "description": ""
        },
        {
            "id": "MONDO:0009770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009770",
            "name": "Michels syndrome",
            "description": ""
        },
        {
            "id": "MIM:257920",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/257920",
            "name": "3MC syndrome 1",
            "description": "3MC syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0060575",
            "label": "3MC syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060576",
            "label": "3MC syndrome 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060577",
            "label": "3MC syndrome 3",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0060577",
        "DOID:0060575",
        "DOID:0060225",
        "DOID:0060576"
    ],
    "unlinked_id_list": []
}