{
    "disease_id": "DOID:0060994",
    "recommended_name": {
        "id": "DOID:0060994",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060994",
        "name": "encephalopathy due to defective mitochondrial and peroxisomal fission 2",
        "description": "A syndrome characterized by delayed psychomotor development, severe hypotonia with inability to walk, microcephaly, and abnormal signals in the basal ganglia that has_material_basis_in homozygous or compound heterozygous mutation in the MFF gene on chromosome 2q36."
    },
    "synonyms": [
        {
            "id": "MONDO:0014905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014905",
            "name": "encephalopathy due to defective mitochondrial and peroxisomal fission 2",
            "description": ""
        },
        {
            "id": "MONDO:0014905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014905",
            "name": "EMPF2",
            "description": ""
        },
        {
            "id": "MONDO:0014905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014905",
            "name": "Leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014905",
            "name": "MFF-associated encephalopathy due to peroxisomal and mitochondrial fission defect",
            "description": ""
        },
        {
            "id": "MONDO:0014905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014905",
            "name": "encephalopathy due to defective mitochondrial and peroxisomal fission 2",
            "description": ""
        },
        {
            "id": "MONDO:0014905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014905",
            "name": "encephalopathy due to defective mitochondrial and peroxisomal fission type 2",
            "description": ""
        },
        {
            "id": "MIM:617086",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617086",
            "name": "Encephalopathy due to defective mitochondrial and peroxisomal fission 2",
            "description": "Encephalopathy due to defective mitochondrial and peroxisomal fission 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060994"
    ],
    "unlinked_id_list": []
}