{
    "disease_id": "DOID:0070239", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013837", 
            "name": "deafness-encephaloneuropathy-obesity-valvulopathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013837", 
            "name": "coenzyme Q10 deficiency, primary, 2; COQ10D2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013837", 
            "name": "COQ10D2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013837", 
            "name": "hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013837", 
            "name": "coenzyme Q10 deficiency, primary, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013837", 
            "name": "coenzyme Q10 deficiency, primary, 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070239", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070239", 
            "name": "COQ10D2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070239", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070239", 
            "name": "hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070239", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070239", 
            "name": "coenzyme Q10 deficiency, primary, 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070239", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070239", 
            "name": "deafness-encephaloneuropathy-obesity-valvulopathy syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070239", 
        "description": "A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of PDSS1 on chromosome 10p12.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070239", 
        "name": "primary coenzyme Q10 deficiency 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070239#disease-associations", 
            "id": "0070239", 
            "database": "Alliance of Genome Resources"
        }
    ]
}