{
    "disease_id": "DOID:0070754",
    "recommended_name": {
        "id": "DOID:0070754",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070754",
        "name": "neurodevelopmental disorder with microcephaly, ataxia, and seizures",
        "description": "An autosomal recessive intellectual developmental disorder characterized by global developmental delay and early-onset seizures that has_material_basis_in homozygous or compound heterozygous mutation in the SARS1 gene on chromosome 1p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070754",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070754",
            "name": "NEDMAS",
            "description": ""
        },
        {
            "id": "MONDO:0060577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060577",
            "name": "neurodevelopmental disorder with microcephaly, ataxia, and seizures",
            "description": ""
        },
        {
            "id": "MONDO:0060577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060577",
            "name": "neurodevelopmental disorder with microcephaly, ataxia, and seizures",
            "description": ""
        },
        {
            "id": "MONDO:0060577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060577",
            "name": "NEDMAS",
            "description": ""
        },
        {
            "id": "MIM:617709",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617709",
            "name": "Neurodevelopmental disorder with microcephaly, ataxia, and seizures",
            "description": "Neurodevelopmental disorder with microcephaly, ataxia, and seizures"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070754"
    ],
    "unlinked_id_list": []
}