{
    "disease_id": "DOID:0070461",
    "recommended_name": {
        "id": "DOID:0070461",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070461",
        "name": "mitochondrial complex V (ATP synthase) deficiency nuclear type 4A",
        "description": "A mitochondrial complex V (ATP synthase) deficiency nuclear type 4 characterized by infantile onset of poor feeding and failure to thrive that may resolve spontaneously or progress to include developmental delay with impaired intellectual development and movement abnormalities that has_material_basis_in autosomal dominant inheritance."
    },
    "synonyms": [
        {
            "id": "DOID:0070461",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070461",
            "name": "MC5DN4A",
            "description": ""
        },
        {
            "id": "MONDO:0957254",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957254",
            "name": "mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A",
            "description": ""
        },
        {
            "id": "MIM:620358",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620358",
            "name": "Mitochondrial complex V deficiency, nuclear type 4A",
            "description": "Mitochondrial complex V deficiency, nuclear type 4A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070461"
    ],
    "unlinked_id_list": []
}