{
    "disease_id": "DOID:0070122", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013482", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013482", 
            "name": "Meckel syndrome, type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013482", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013482", 
            "name": "Meckel syndrome caused by mutation in TCTN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013482", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013482", 
            "name": "Meckel-Gruber syndrome, type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013482", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013482", 
            "name": "MKS8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013482", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013482", 
            "name": "TCTN2 Meckel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013482", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013482", 
            "name": "Meckel syndrome, type 8; MKS8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070122", 
            "name": "MKS8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070122", 
            "name": "Meckel-Gruber syndrome, type 8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070122", 
        "description": "A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TCTN2 on chromosome 12q24.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070122", 
        "name": "Meckel syndrome 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070122#disease-associations", 
            "id": "0070122", 
            "database": "Alliance of Genome Resources"
        }
    ]
}