{
    "disease_id": "DOID:11105", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007639", 
            "name": "pigmentary retinal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007639", 
            "name": "retinitis punctata albescens"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11105", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11105", 
            "name": "Pigmentary retinal dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11105", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11105", 
            "name": "retinitis punctata albescens"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11105", 
        "description": "A fundus dystrophy that is characterized by discrete uniform white dots over the entire fundus with greatest density in the midperiphery and no macular involvement.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11105", 
        "name": "fundus albipunctatus"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/11105#disease-associations", 
            "id": "11105", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
