{
    "disease_id": "DOID:0112246",
    "recommended_name": {
        "id": "DOID:0112246",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112246",
        "name": "glutaric acidemia type 3",
        "description": "A peroxisomal disease characterized by isolated accumulation of glutaric acid in the absence of other clinical phenotype that has_material_basis_in homozygous or compound heterozygous mutation in the SUGCT gene on chromosome 7p14.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112246",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112246",
            "name": "GA III",
            "description": ""
        },
        {
            "id": "DOID:0112246",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112246",
            "name": "GA3",
            "description": ""
        },
        {
            "id": "DOID:0112246",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112246",
            "name": "glutaric aciduria 3",
            "description": ""
        },
        {
            "id": "DOID:0112246",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112246",
            "name": "glutaric aciduria III",
            "description": ""
        },
        {
            "id": "DOID:0112246",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112246",
            "name": "glutaric aciduria type 3",
            "description": ""
        },
        {
            "id": "DOID:0112246",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112246",
            "name": "glutaryl-CoA oxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric acidemia type 3",
            "description": "Glutaryl-CoA oxidase deficiency is a peroxisomal disorder leading to glutaric aciduria. The prevalence is unknown. There is no distinctive phenotype associated with this disorder and one of the reported cases was asymptomatic. Transmission appears to be autosomal recessive."
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "SUGCT glutaric aciduria (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric acidemia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric aciduria (disease) caused by mutation in SUGCT",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric aciduria type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaryl-CoA oxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "GA III",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "GA3",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "Ga 3",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric acidemia type III",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric aciduria 3",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric aciduria III",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaric aciduria type III",
            "description": ""
        },
        {
            "id": "MONDO:0009283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009283",
            "name": "glutaryl-Coa oxidase deficiency",
            "description": ""
        },
        {
            "id": "MIM:231690",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/231690",
            "name": "Glutaric aciduria 3",
            "description": "Glutaric aciduria 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112246"
    ],
    "unlinked_id_list": []
}