{
    "disease_id": "DOID:0070120", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012848", 
            "name": "Meckel syndrome, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012848", 
            "name": "Meckel syndrome, type 6; MKS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012848", 
            "name": "Meckel syndrome caused by mutation in CC2D2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012848", 
            "name": "MKS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012848", 
            "name": "Meckel-Gruber syndrome, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012848", 
            "name": "CC2D2A Meckel syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070120", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070120", 
            "name": "MKS6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070120", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070120", 
            "name": "Meckel-Gruber syndrome, type 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070120", 
        "description": "A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070120", 
        "name": "Meckel syndrome 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070120#disease-associations", 
            "id": "0070120", 
            "database": "Alliance of Genome Resources"
        }
    ]
}