{
    "disease_id": "DOID:0111254",
    "recommended_name": {
        "id": "DOID:0111254",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111254",
        "name": "glutaric acidemia I",
        "description": "An organic acidemia characterized by impaired lysine, hydroxylysine, and tryptophan metabolism, increased urinary excretion of glutaric acid, and accumulation of 3-hydroxyglutaric and glutaric acid, resulting in striatal injury and a severe dystonic dyskinetic movement disorder that has_material_basis_in homozygous or compound heterozygous mutation in the GCDH gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0111254",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111254",
            "name": "GA1",
            "description": ""
        },
        {
            "id": "DOID:0111254",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111254",
            "name": "glutaric academia type 1",
            "description": ""
        },
        {
            "id": "DOID:0111254",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111254",
            "name": "glutaric aciduria 1",
            "description": ""
        },
        {
            "id": "DOID:0111254",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111254",
            "name": "glutaric aciduria type I",
            "description": ""
        },
        {
            "id": "DOID:0111254",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111254",
            "name": "glutaryl-coA dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111254",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111254",
            "name": "glutaryl-coenzyme A dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaryl-CoA dehydrogenase deficiency",
            "description": "Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder."
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "GA1",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "GCDHD",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaric acidemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaric aciduria type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaric aciduria, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaricaciduria, type I",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaryl-CoA dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaryl-coenzyme A dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaric acidemia 1",
            "description": ""
        },
        {
            "id": "MONDO:0009281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009281",
            "name": "glutaric acidemia type I",
            "description": ""
        },
        {
            "id": "MIM:231670",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/231670",
            "name": "Glutaric aciduria 1",
            "description": "Glutaric aciduria 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111254"
    ],
    "unlinked_id_list": []
}