{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012695", 
            "name": "Meckel syndrome, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012695", 
            "name": "RPGRIP1L Meckel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012695", 
            "name": "Meckel-Gruber syndrome, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012695", 
            "name": "Meckel syndrome, type 5; MKS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012695", 
            "name": "MKS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012695", 
            "name": "Meckel syndrome caused by mutation in RPGRIP1L"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070119", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070119", 
            "name": "MKS5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070119", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070119", 
            "name": "Meckel-Gruber syndrome, type 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070119", 
        "description": "A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of RPGRIP1L on chromosome 16q12.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070119", 
        "name": "Meckel syndrome 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611561", 
            "id": "611561", 
            "database": "MIM"
        }
    ]
}