{
    "disease_id": "DOID:0070122",
    "recommended_name": {
        "id": "DOID:0070122",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070122",
        "name": "Meckel syndrome 8",
        "description": "A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TCTN2 on chromosome 12q24.31."
    },
    "synonyms": [
        {
            "id": "DOID:0070122",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070122",
            "name": "MKS8",
            "description": ""
        },
        {
            "id": "DOID:0070122",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070122",
            "name": "Meckel-Gruber syndrome, type 8",
            "description": ""
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "Meckel syndrome, type 8",
            "description": "Any Meckel syndrome in which the cause of the disease is a mutation in the TCTN2 gene."
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "Meckel syndrome 8",
            "description": ""
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "Meckel syndrome caused by mutation in TCTN2",
            "description": ""
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "Meckel-Gruber syndrome, type 8",
            "description": ""
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "Meckel syndrome, type 8",
            "description": ""
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "MKS8",
            "description": ""
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "TCTN2 Meckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013482",
            "name": "Meckel syndrome, type 8; MKS8",
            "description": ""
        },
        {
            "id": "MIM:613885",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613885",
            "name": "Meckel syndrome 8",
            "description": "Meckel syndrome 8"
        }
    ]
}