{
    "disease_id": "DOID:0110018", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013406", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013406", 
            "name": "age related macular degeneration type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013406", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013406", 
            "name": "ARMD6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013406", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013406", 
            "name": "age-related macular degeneration caused by mutation in RAX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013406", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013406", 
            "name": "macular degeneration, age-related, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013406", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013406", 
            "name": "RAX2 age-related macular degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013406", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013406", 
            "name": "macular Degeneration, age-related, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013406", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013406", 
            "name": "macular degeneration, age-related, 6; ARMD6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110018", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110018", 
            "name": "ARMD6"
        }, 
        {
            "url": "https://www.omim.org/entry/613757", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613757", 
            "name": "Macular degeneration, age-related, 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110018", 
        "description": "An age related macular degeneration conferred by heterozygous mutation in the RAXL1 gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110018", 
        "name": "age related macular degeneration 6"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613757", 
            "id": "613757", 
            "database": "MIM"
        }
    ]
}
