{
    "disease_id": "DOID:0060358",
    "recommended_name": {
        "id": "DOID:0060358",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060358",
        "name": "multiple acyl-CoA dehydrogenase deficiency",
        "description": "An inherited metabolic disorder characterized by the body's inability to break down proteins and fats to produce energy. It is a disorder of fatty acid, amino acid, and choline metabolism and has an autosomal recessive inheritance pattern. It has_material_basis_in mutations in the ETFA, ETFB and ETFDH genes. It presents three clinical phenotypes: a neonatal-onset form with congenital anomalies (type I), a neonatal-onset form without congenital anomalies (type II), and a late-onset form (type III). The neonatal-onset forms are usually fatal."
    },
    "synonyms": [
        {
            "id": "DOID:0060358",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060358",
            "name": "electron transfer flavoprotein ubiquinone oxidoreductase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060358",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060358",
            "name": "MAD deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060358",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060358",
            "name": "MADD",
            "description": ""
        },
        {
            "id": "DOID:0060358",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060358",
            "name": "electron transfer flavoprotein deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060358",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060358",
            "name": "glutaric acidemia type 2",
            "description": ""
        },
        {
            "id": "DOID:0060358",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060358",
            "name": "glutaric aciduria type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "multiple acyl-CoA dehydrogenase deficiency",
            "description": "A disorder of fatty acid and amino acid oxidation, caused by mutations in ETFDH, ETFA, or ETFB, and is a clinically heterogeneous disorder ranging from a severe neonatal presentation with metabolic acidosis, cardiomyopathy and liver disease, to a mild childhood/adult disease with episodic metabolic decompensation, muscle weakness, and respiratory failure."
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "Glutaric Aciduria Type II",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "MAD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "MADD",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "electron transfer flavoprotein deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia type II",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric aciduria type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric aciduria, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "multiple acyl Coenzyme A dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "multiple acyl-CoA dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "Etfa deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "Etfb deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "Etfdh deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia 2A",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia 2B",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia 2C",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia IIA",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia IIB",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "glutaric acidemia IIC",
            "description": ""
        },
        {
            "id": "MONDO:0009282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009282",
            "name": "EMA",
            "description": ""
        },
        {
            "id": "MIM:231680",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/231680",
            "name": "Glutaric aciduria 2C",
            "description": "Glutaric aciduria 2C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060358"
    ],
    "unlinked_id_list": []
}