{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "Doyne honeycomb degeneration of retina"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "Malattia leventinese"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "dominant radial drusen"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "DHRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "dominant drusen"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "Doyne honeycomb retinal dystrophy; DHRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "drusen, radial, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "DHD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007471", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007471", 
            "name": "familial drusen"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060745", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060745", 
            "name": "DHRD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060745", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060745", 
            "name": "Doyne honeycomb degeneration of retina"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060745", 
        "description": "A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium in the posterior pole of the eye in a honeycomb pattern and that has_material_basis_in mutations in the EFEMP1 gene on chromosome 2p16.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060745", 
        "name": "Doyne honeycomb retinal dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/126600", 
            "id": "126600", 
            "database": "MIM"
        }
    ]
}