{
    "disease_id": "DOID:0110004",
    "recommended_name": {
        "id": "DOID:0110004",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110004",
        "name": "3-methylglutaconic aciduria type 3",
        "description": "A 3-methylglutaconic aciduria that has_material_basis_in mutation in the OPA3 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "3-methylglutaconic aciduria type III",
            "description": ""
        },
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "Costeff optic atrophy syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "Costeff syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "Iraqi-Jewish optic atrophy plus",
            "description": ""
        },
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "MGA3",
            "description": ""
        },
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "autosomal recessive optic atrophy plus syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "autosomal recessive optic atrophy type 3",
            "description": ""
        },
        {
            "id": "DOID:0110004",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110004",
            "name": "infantile optic atrophy with chorea and spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "3-methylglutaconic aciduria type 3",
            "description": "3-methylglutaconic aciduria type III (MGA III) is an organic aciduria characterized by the association of optic atrophy and choreoathetosis with 3-methylglutaconic aciduria."
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "OPA3 defect",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "3-methylglutaconic aciduria caused by mutation in OPA3",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "Costeff optic atrophy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "Costeff syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "MGA3",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "OPA3 3-methylglutaconic aciduria",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "autosomal recessive optic atrophy plus syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "autosomal recessive optic atrophy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "infantile optic atrophy with chorea and spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "3-alpha methylglutaconic aciduria type III",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "3-methylglutaconic aciduria, type III",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "Iraqi Jewish optic atrophy plus",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "MGA type III",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "MGCA3",
            "description": ""
        },
        {
            "id": "MONDO:0009787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009787",
            "name": "optic atrophy infantile with chorea and spastic paraplegia",
            "description": ""
        },
        {
            "id": "MIM:258501",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/258501",
            "name": "3-methylglutaconic aciduria 3",
            "description": "3-methylglutaconic aciduria 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110004"
    ],
    "unlinked_id_list": []
}