{
    "disease_id": "DOID:0111028",
    "recommended_name": {
        "id": "DOID:0111028",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111028",
        "name": "hemochromatosis type 4",
        "description": "A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32."
    },
    "synonyms": [
        {
            "id": "DOID:0111028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111028",
            "name": "HFE4",
            "description": ""
        },
        {
            "id": "DOID:0111028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111028",
            "name": "autosomal dominant hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "DOID:0111028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111028",
            "name": "ferroportin disease",
            "description": ""
        },
        {
            "id": "DOID:0111028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111028",
            "name": "hemochromatosis due to defect in ferroportin",
            "description": ""
        },
        {
            "id": "MONDO:0011631",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011631",
            "name": "hemochromatosis type 4",
            "description": "A form of rare hemochromatosis (HC) characterized by increased transferrin saturation and hepatocellular iron deposition with distribution patterns and clinical features indistinguishable from patients with other types of HC."
        },
        {
            "id": "MONDO:0011631",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011631",
            "name": "Ferroportin Disease",
            "description": ""
        },
        {
            "id": "MONDO:0011631",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011631",
            "name": "HFE4",
            "description": ""
        },
        {
            "id": "MONDO:0011631",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011631",
            "name": "SLC40A1 hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0011631",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011631",
            "name": "ferroportin disease",
            "description": ""
        },
        {
            "id": "MONDO:0011631",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011631",
            "name": "hereditary hemochromatosis caused by mutation in SLC40A1",
            "description": ""
        },
        {
            "id": "MONDO:0011631",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011631",
            "name": "hemochromatosis, type 4",
            "description": ""
        },
        {
            "id": "MIM:606069",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606069",
            "name": "Hemochromatosis 4",
            "description": "Hemochromatosis 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111028"
    ],
    "unlinked_id_list": []
}