{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013986", 
            "name": "combined oxidative phosphorylation defect type 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013986", 
            "name": "combined oxidative phosphorylation deficiency caused by mutation in FARS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013986", 
            "name": "combined oxidative phosphorylation deficiency 14; COXPD14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013986", 
            "name": "COXPD14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013986", 
            "name": "combined oxidative phosphorylation deficiency type 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013986", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013986", 
            "name": "FARS2 combined oxidative phosphorylation deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111477", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111477", 
            "name": "COXPD14"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111477", 
        "description": "A combined oxidative phosphorylation deficiency characterized by neonatal onset of global developmental delay, refractory seizures, and lactic acidosis that has_material_basis_in homozygous or compound heterozygous mutation in FARS2 on chromosome 6p25.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111477", 
        "name": "combined oxidative phosphorylation deficiency 14"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614946", 
            "id": "614946", 
            "database": "MIM"
        }
    ]
}