{
    "disease_id": "DOID:0111031", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "hemochromatosis, type 5; HFE5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "HFE5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "FTH1-associated iron overload"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "FTH1-related iron overload"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "hemochromatosis, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "iron overload, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "FTH1 hereditary hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014225", 
            "name": "hereditary hemochromatosis caused by mutation in FTH1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111031", 
            "name": "FTH1-associated iron overload"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111031", 
            "name": "FTH1-related iron overload"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111031", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111031", 
            "name": "HFE5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111031", 
        "description": "A hemochromatosis that has_material_basis_in heterozygous mutation in the FTH1 gene on chromosome 11q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111031", 
        "name": "hemochromatosis type 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111031#disease-associations", 
            "id": "0111031", 
            "database": "Alliance of Genome Resources"
        }
    ]
}