{
    "disease_id": "DOID:0061116",
    "recommended_name": {
        "id": "DOID:0061116",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061116",
        "name": "Carey-Fineman-Ziter syndrome 2",
        "description": "A Carey-Fineman-Ziter syndrome characterized by motor developmental delay, facial weakness, hypotonia, growth restriction, feeding difficulties, and velopharyngeal insufficiency that has_material_basis_inhomozygous mutation in MYMX gene on chromosome 6p21."
    },
    "synonyms": [
        {
            "id": "DOID:0061116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061116",
            "name": "CFZS2",
            "description": ""
        },
        {
            "id": "MONDO:0100292",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100292",
            "name": "Carey-Fineman-Ziter syndrome 2",
            "description": "Any Carey-Fineman-Ziter syndrome in which the cause of the disease is a mutation in the MYMX gene."
        },
        {
            "id": "MONDO:0100292",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100292",
            "name": "CFZS2",
            "description": ""
        },
        {
            "id": "MIM:619941",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619941",
            "name": "Carey-Fineman-Ziter syndrome 2",
            "description": "Carey-Fineman-Ziter syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061116"
    ],
    "unlinked_id_list": []
}