{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "hereditary hemochromatosis caused by mutation in SLC40A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "hemochromatosis due to defect in ferroportin"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "hemochromatosis, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "hemochromatosis, type 4; HFE4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "SLC40A1 hereditary hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "hemochromatosis, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "HFE4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "autosomal dominant hereditary hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011631", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011631", 
            "name": "ferroportin disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111028", 
            "name": "HFE4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111028", 
            "name": "autosomal dominant hereditary hemochromatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111028", 
            "name": "ferroportin disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111028", 
            "name": "hemochromatosis due to defect in ferroportin"
        }, 
        {
            "url": "https://www.omim.org/entry/606069", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:606069", 
            "name": "Hemochromatosis 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111028", 
        "description": "A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111028", 
        "name": "hemochromatosis type 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/606069", 
            "id": "606069", 
            "database": "MIM"
        }
    ]
}