{
    "disease_id": "DOID:0070121", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "NPHP3-related Meckel-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "Meckel syndrome, type 7; MKS7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "Meckel syndrome type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "Meckel-Gruber syndrome, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "Meckel-like syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "MKS7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "Goldston syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009966", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009966", 
            "name": "Meckel syndrome, type 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070121", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070121", 
            "name": "MKS7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070121", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070121", 
            "name": "Meckel-Gruber syndrome, type 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070121", 
        "description": "A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of NPHP3 on chromosome 3q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070121", 
        "name": "Meckel syndrome 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070121#disease-associations", 
            "id": "0070121", 
            "database": "Alliance of Genome Resources"
        }
    ]
}