{
    "disease_id": "DOID:0070120",
    "recommended_name": {
        "id": "DOID:0070120",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070120",
        "name": "Meckel syndrome 6",
        "description": "A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32."
    },
    "synonyms": [
        {
            "id": "DOID:0070120",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070120",
            "name": "MKS6",
            "description": ""
        },
        {
            "id": "DOID:0070120",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070120",
            "name": "Meckel-Gruber syndrome, type 6",
            "description": ""
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "Meckel syndrome, type 6",
            "description": "Any Meckel syndrome in which the cause of the disease is a mutation in the CC2D2A gene."
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "Meckel syndrome, type 6; MKS6",
            "description": ""
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "Meckel syndrome caused by mutation in CC2D2A",
            "description": ""
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "Meckel syndrome, type 6",
            "description": ""
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "Meckel syndrome 6",
            "description": ""
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "MKS6",
            "description": ""
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "Meckel-Gruber syndrome, type 6",
            "description": ""
        },
        {
            "id": "MONDO:0012848",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012848",
            "name": "CC2D2A Meckel syndrome",
            "description": ""
        },
        {
            "id": "MIM:612284",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612284",
            "name": "Meckel syndrome 6",
            "description": "Meckel syndrome 6"
        }
    ]
}