{
    "disease_id": "DOID:0110003",
    "recommended_name": {
        "id": "DOID:0110003",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110003",
        "name": "3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia",
        "description": "A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the CLPB gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110003",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110003",
            "name": "3-methylglutaconic aciduria type 7",
            "description": ""
        },
        {
            "id": "DOID:0110003",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110003",
            "name": "3-methylglutaconic aciduria type VII",
            "description": ""
        },
        {
            "id": "DOID:0110003",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110003",
            "name": "MEGCANN",
            "description": ""
        },
        {
            "id": "DOID:0110003",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110003",
            "name": "MGA7",
            "description": ""
        },
        {
            "id": "DOID:0110003",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110003",
            "name": "MGCA7",
            "description": ""
        }
    ]
}