{
    "disease_id": "DOID:0081051",
    "recommended_name": {
        "id": "DOID:0081051",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081051",
        "name": "microcephaly, growth deficiency, seizures, and brain malformations",
        "description": "A syndrome that is characterized by intrauterine growth retardation, postnatal growth deficiency with severe microcephaly, and poor or absent psychomotor development, and that has_material_basis_in homozygous mutation in the WDR4 gene on chromosome 21q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0032690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032690",
            "name": "microcephaly, growth deficiency, seizures, and brain malformations",
            "description": ""
        },
        {
            "id": "MONDO:0032690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032690",
            "name": "MIGSB",
            "description": ""
        },
        {
            "id": "MIM:618346",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618346",
            "name": "Microcephaly, growth deficiency, seizures, and brain malformations",
            "description": "Microcephaly, growth deficiency, seizures, and brain malformations"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081051"
    ],
    "unlinked_id_list": []
}