{
    "disease_id": "DOID:0070347", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013726", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013726", 
            "name": "lethal encephalopathy due to mitochondrial and peroxisomal fission defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013726", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013726", 
            "name": "encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013726", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013726", 
            "name": "EMPF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013726", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013726", 
            "name": "encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission; EMPF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013726", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013726", 
            "name": "EMPF1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013726", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013726", 
            "name": "encephalopathy due to defective mitochondrial and peroxisomal fission 1; EMPF1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070347", 
        "description": "A syndrome that has_material_basis_in heterozygous mutation in the DNM1L gene, and is characterized by delayed psychomotor development and has_symptom hypotonia that may lead to death in childhood.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070347", 
        "name": "encephalopathy due to defective mitochondrial and peroxisomal fission 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070347#disease-associations", 
            "id": "0070347", 
            "database": "Alliance of Genome Resources"
        }
    ]
}