{
    "disease_id": "DOID:0061296",
    "recommended_name": {
        "id": "DOID:0061296",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061296",
        "name": "Meckel syndrome 11",
        "description": "A Meckel syndrome that has_material_basis_in homozygous mutation in the TMEM231 gene on chromosome 16q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "Meckel syndrome, type 11",
            "description": "Any Meckel syndrome in which the cause of the disease is a mutation in the TMEM231 gene."
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "Meckel syndrome caused by mutation in TMEM231",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "Meckel syndrome, type 11",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "TMEM231 Meckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "meckel syndrome 11",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "MKS11",
            "description": ""
        },
        {
            "id": "MIM:615397",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615397",
            "name": "Meckel syndrome 11",
            "description": "Meckel syndrome 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061296"
    ],
    "unlinked_id_list": []
}