{
    "disease_id": "DOID:0050711",
    "recommended_name": {
        "id": "DOID:0050711",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050711",
        "name": "aceruloplasminemia",
        "description": "An iron metabolism disease that has_material_basis_in a mutation in the ceruloplasmin gene characterized by progressive neurodegeneration of the retina and basal ganglia and diabetes mellitus."
    },
    "synonyms": [
        {
            "id": "MONDO:0011426",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011426",
            "name": "aceruloplasminemia",
            "description": "An adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms."
        },
        {
            "id": "MONDO:0011426",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011426",
            "name": "cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0011426",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011426",
            "name": "aceruloplasminemia",
            "description": ""
        },
        {
            "id": "MONDO:0011426",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011426",
            "name": "hereditary ceruloplasmin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011426",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011426",
            "name": "hypoceruloplasminemia, hereditary",
            "description": ""
        },
        {
            "id": "MONDO:0011426",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011426",
            "name": "familial apoceruloplasmin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011426",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011426",
            "name": "systemic hemosiderosis due to aceruloplasminemia",
            "description": ""
        },
        {
            "id": "MIM:604290",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604290",
            "name": "Aceruloplasminemia",
            "description": "Aceruloplasminemia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050711"
    ],
    "unlinked_id_list": []
}