{
    "disease_id": "DOID:0060844", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "Norrie syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "Episkopi blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "fetal iritis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "nd"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "atrophia bulborum hereditaria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "Norrie-Warburg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "Anderson-Warburg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "pseudoglioma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "Norrie-Warburg disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "NDP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010691", 
            "name": "Norrie disease; nd"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060844", 
            "name": "Episkopi blindness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060844", 
            "name": "Norrie-Warburg disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060844", 
            "name": "atrophia bulborum hereditaria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060844", 
        "description": "A syndrome characterized by degenerative and proliferative changes of the neuroretina resulting in congenital blindness along with progressive mental disorders in about 50% of patients and sensorineural deafness in about 33% of patients, and that has_material_basis_in mutation in the NDP gene on chromosome Xp11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060844", 
        "name": "Norrie disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/310600", 
            "id": "310600", 
            "database": "MIM"
        }
    ]
}