{
    "disease_id": "DOID:0061291",
    "recommended_name": {
        "id": "DOID:0061291",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061291",
        "name": "Galloway-Mowat syndrome 8",
        "description": "A Galloway-Mowat syndrome characterized by impaired psychomotor development, poor overall growth with microcephaly, and early-onset progressive nephrotic syndrome associated with focal segmental glomerulosclerosis on renal biopsy that has_material_basis_in homozygous mutation in the NUP133 gene on chromosome 1q42."
    },
    "synonyms": [
        {
            "id": "MONDO:0032693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032693",
            "name": "Galloway-Mowat syndrome 8",
            "description": ""
        },
        {
            "id": "MONDO:0032693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032693",
            "name": "GAMOS8",
            "description": ""
        },
        {
            "id": "MIM:618349",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618349",
            "name": "Galloway-Mowat syndrome 8",
            "description": "Galloway-Mowat syndrome 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061291"
    ],
    "unlinked_id_list": []
}