{
    "disease_id": "DOID:0070420",
    "recommended_name": {
        "id": "DOID:0070420",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070420",
        "name": "developmental delay, hypotonia, and impaired language",
        "description": "An autosomal dominant intellectual developmental disorder characterized by variably impaired intellectual development usually with hypotonia, mild motor delay, and language difficulties that has_material_basis_in heterozygous mutation in the FBXW7 gene on chromosome 4q31."
    },
    "synonyms": [
        {
            "id": "DOID:0070420",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070420",
            "name": "DEDHIL",
            "description": ""
        },
        {
            "id": "MONDO:0859280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859280",
            "name": "developmental delay, hypotonia, and impaired language",
            "description": ""
        },
        {
            "id": "MIM:620012",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620012",
            "name": "Developmental delay, hypotonia, and impaired language",
            "description": "Developmental delay, hypotonia, and impaired language"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070420"
    ],
    "unlinked_id_list": []
}