{
    "disease_id": "DOID:0112072", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012624", 
            "name": "acyl-CoA dehydrogenase 9 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012624", 
            "name": "Acad9 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012624", 
            "name": "mitochondrial complex I deficiency due to ACAD9 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012624", 
            "name": "mitochondrial Complex 1 deficiency due to Acad9 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112072", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112072", 
            "name": "Acyl-CoA dehydrogenase 9 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112072", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112072", 
            "name": "ACAD9 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112072", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112072", 
            "name": "MC1DN20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112072", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112072", 
            "name": "mitochondrial complex 1 deficiency due to ACAD9 deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/611126", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:611126", 
            "name": "Mitochondrial complex I deficiency, nuclear type 20"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112072", 
        "description": "A nuclear type mitochondrial complex I deficiency characterized by infantile onset of acute metabolic acidosis, hypertrophic cardiomyopathy, and muscle weakness associated with deficiency of mitochondrial complex I activity in muscle, liver, and fibroblasts that has_material_basis_in homozygous or compound heterozygous mutation in ACAD9 on chromosome 3q21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112072", 
        "name": "nuclear type mitochondrial complex I deficiency 20"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611126", 
            "id": "611126", 
            "database": "MIM"
        }
    ]
}