{
    "disease_id": "DOID:0111031",
    "recommended_name": {
        "id": "DOID:0111031",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111031",
        "name": "hemochromatosis type 5",
        "description": "A hemochromatosis that has_material_basis_in heterozygous mutation in the FTH1 gene on chromosome 11q12."
    },
    "synonyms": [
        {
            "id": "DOID:0111031",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111031",
            "name": "FTH1-associated iron overload",
            "description": ""
        },
        {
            "id": "DOID:0111031",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111031",
            "name": "FTH1-related iron overload",
            "description": ""
        },
        {
            "id": "DOID:0111031",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111031",
            "name": "HFE5",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "hemochromatosis type 5",
            "description": "Any hereditary hemochromatosis in which the cause of the disease is a mutation in the FTH1 gene."
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "hemochromatosis, type 5; HFE5",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "HFE5",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "FTH1-associated iron overload",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "FTH1-related iron overload",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "hemochromatosis, type 5",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "iron overload, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "FTH1 hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0014225",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014225",
            "name": "hereditary hemochromatosis caused by mutation in FTH1",
            "description": ""
        },
        {
            "id": "MIM:615517",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615517",
            "name": "Hemochromatosis 5",
            "description": "Hemochromatosis 5"
        }
    ]
}