{
    "disease_id": "DOID:0070121",
    "recommended_name": {
        "id": "DOID:0070121",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070121",
        "name": "Meckel syndrome 7",
        "description": "A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the NPHP3 gene on chromosome 3q22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070121",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070121",
            "name": "MKS7",
            "description": ""
        },
        {
            "id": "DOID:0070121",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070121",
            "name": "Meckel-Gruber syndrome, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "NPHP3-related Meckel-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "Goldston syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "MKS7",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "Meckel syndrome type 7",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "Meckel-Gruber syndrome, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "Meckel-like syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "NPHP3-related Meckel-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "Meckel syndrome 7",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "Meckel syndrome, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0009966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009966",
            "name": "renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst",
            "description": ""
        },
        {
            "id": "MIM:267010",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/267010",
            "name": "Meckel syndrome 7",
            "description": "Meckel syndrome 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070121"
    ],
    "unlinked_id_list": []
}