{
    "disease_id": "DOID:0070653",
    "recommended_name": {
        "id": "DOID:0070653",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070653",
        "name": "Fliedner-Zweier syndrome",
        "description": "A syndromic intellectual disability characterized by variable manifestations including mild intellectual disability, seizures, behavioral abnormalities, and skeletal and structural anomalies that has_material_basis_in heterozygous mutation in the SCAF4 gene on chromosome 21q22."
    },
    "synonyms": [
        {
            "id": "DOID:0070653",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070653",
            "name": "SCAF4-related syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0957787",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957787",
            "name": "Fliedner-Zweier syndrome",
            "description": ""
        },
        {
            "id": "MIM:620511",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620511",
            "name": "Fliedner-Zweier syndrome",
            "description": "Fliedner-Zweier syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070653"
    ],
    "unlinked_id_list": []
}