{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011216", 
            "name": "HJV hemochromatosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011216", 
            "name": "HFE2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011216", 
            "name": "hemochromatosis, juvenile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011216", 
            "name": "hemochromatosis, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011216", 
            "name": "hemochromatosis, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011216", 
            "name": "hemochromatosis, type 2A; HFE2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011216", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011216", 
            "name": "hemochromatosis type 2 caused by mutation in HJV"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111027", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111027", 
            "name": "HFE2A"
        }, 
        {
            "url": "https://www.omim.org/entry/602390", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:602390", 
            "name": "Hemochromatosis 2A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111027", 
        "description": "A hemochromatosis type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the HJV gene on chromosome 1q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111027", 
        "name": "hemochromatosis type 2A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/602390", 
            "id": "602390", 
            "database": "MIM"
        }
    ]
}