{
    "disease_id": "DOID:0050778",
    "recommended_name": {
        "id": "DOID:0050778",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050778",
        "name": "Meckel syndrome",
        "description": "A ciliopathy that is characterized by renal cystic dysplasia, occipital encephalocele, polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia."
    },
    "synonyms": [
        {
            "id": "DOID:0050778",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050778",
            "name": "Meckel-Gruber syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel syndrome, type 1",
            "description": "Any Meckel syndrome in which the cause of the disease is a mutation in the MKS1 gene."
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "MKS1",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "MKS1 Meckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel syndrome caused by mutation in MKS1",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel syndrome, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel-Gruber syndrome, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Dysencephalia Splanchnocystica",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Dysencephalia splachnocystica",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Gruber syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "MKS",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel Gruber syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel syndrome type1",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Meckel-Gruber syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009571",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009571",
            "name": "Mes",
            "description": ""
        },
        {
            "id": "MIM:249000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/249000",
            "name": "Meckel syndrome 1",
            "description": "Meckel syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0061294",
            "label": "Meckel syndrome 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0061295",
            "label": "Meckel syndrome 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0061296",
            "label": "Meckel syndrome 11",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0061297",
            "label": "Meckel syndrome 12",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070115",
            "label": "Meckel syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070116",
            "label": "Meckel syndrome 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070117",
            "label": "Meckel syndrome 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070118",
            "label": "Meckel syndrome 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070119",
            "label": "Meckel syndrome 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070120",
            "label": "Meckel syndrome 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070121",
            "label": "Meckel syndrome 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070122",
            "label": "Meckel syndrome 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070703",
            "label": "Meckel syndrome 14",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080253",
            "label": "Meckel syndrome 13",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070118",
        "DOID:0070116",
        "DOID:0080253",
        "DOID:0070119",
        "DOID:0061296",
        "DOID:0050778",
        "DOID:0061295",
        "DOID:0070121",
        "DOID:0070122",
        "DOID:0070120",
        "DOID:0061294",
        "DOID:0070115",
        "DOID:0070117",
        "DOID:0061297",
        "DOID:0070703"
    ],
    "unlinked_id_list": []
}