{
    "disease_id": "DOID:0060364",
    "recommended_name": {
        "id": "DOID:0060364",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060364",
        "name": "Galloway-Mowat syndrome 1",
        "description": "A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25."
    },
    "synonyms": [
        {
            "id": "DOID:0060364",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060364",
            "name": "Galloway syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060364",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060364",
            "name": "microcephaly, hiatal hernia and nephrotic syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060364",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060364",
            "name": "nephrosis-microcephaly syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060364",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060364",
            "name": "nephrosis-neuronal dysmigration syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060364",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060364",
            "name": "SCAR5",
            "description": ""
        },
        {
            "id": "DOID:0060364",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060364",
            "name": "autosomal recessive spinocerebellar ataxia 5",
            "description": ""
        },
        {
            "id": "MONDO:0033005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033005",
            "name": "Galloway-Mowat syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0033005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033005",
            "name": "Galloway-Mowat syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0033005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033005",
            "name": "GAMOS1",
            "description": ""
        },
        {
            "id": "MONDO:0033005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033005",
            "name": "cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities",
            "description": ""
        },
        {
            "id": "MONDO:0033005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033005",
            "name": "spinocerebellar ataxia, autosomal recessive 5",
            "description": ""
        },
        {
            "id": "MIM:251300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/251300",
            "name": "Galloway-Mowat syndrome 1",
            "description": "Galloway-Mowat syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060364"
    ],
    "unlinked_id_list": []
}