{
    "disease_id": "DOID:0061158",
    "recommended_name": {
        "id": "DOID:0061158",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061158",
        "name": "Kariminejad neurodevelopmental syndrome",
        "description": "An autosomal recessive intellectual developmental disorder characterized by global developmental delay with delayed walking by a few years, speech delay, and impaired intellectual development that has_material_basis_in homozygous mutation in the RBSN gene on chromosome 3p25."
    },
    "synonyms": [
        {
            "id": "MONDO:0975795",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0975795",
            "name": "Kariminejad neurodevelopmental syndrome",
            "description": ""
        },
        {
            "id": "MIM:620937",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620937",
            "name": "Kariminejad neurodevelopmental syndrome",
            "description": "Kariminejad neurodevelopmental syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061158"
    ],
    "unlinked_id_list": []
}