{
    "disease_id": "DOID:0060358", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric acidemia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric acidemia 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "MADD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric acidemia 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric acidemia 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "multiple acyl Coenzyme A dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "Etfa deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "ethylmalonic-Adipicaciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "Etfdh deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "Etfb deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "EMA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric aciduria type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "MAD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "Ga 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric acidemia type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "electron transfer flavoprotein deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric aciduria 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "electron transfer flavoprotein ubiquinone oxidoreductase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "multiple acyl-CoA dehydrogenase deficiency; MADD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric aciduria, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009282", 
            "name": "glutaric acidemia 2C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060358", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060358", 
            "name": "electron transfer flavoprotein ubiquinone oxidoreductase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060358", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060358", 
            "name": "MAD deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060358", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060358", 
            "name": "MADD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060358", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060358", 
            "name": "electron transfer flavoprotein deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060358", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060358", 
            "name": "glutaric acidemia type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060358", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060358", 
            "name": "glutaric aciduria type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060358", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060358", 
        "name": "multiple acyl-CoA dehydrogenase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060358#disease-associations", 
            "id": "0060358", 
            "database": "Alliance of Genome Resources"
        }
    ]
}