{
    "disease_id": "DOID:0070244", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014562", 
            "name": "neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014562", 
            "name": "coenzyme Q10 deficiency, primary, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014562", 
            "name": "coenzyme Q10 deficiency, primary, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014562", 
            "name": "COQ10D7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014562", 
            "name": "COQ4-related neonatal encephalomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014562", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014562", 
            "name": "coenzyme Q10 deficiency, primary, 7; COQ10D7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070244", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070244", 
            "name": "neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070244", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070244", 
            "name": "COQ10D7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070244", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070244", 
            "name": "COQ4-related neonatal encephalomyopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070244", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070244", 
            "name": "coenzyme Q10 deficiency, primary, 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070244", 
        "description": "A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of COQ4 on chromosome 9q34.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070244", 
        "name": "primary coenzyme Q10 deficiency 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070244#disease-associations", 
            "id": "0070244", 
            "database": "Alliance of Genome Resources"
        }
    ]
}