{
    "disease_id": "DOID:0111228", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007176", 
            "name": "helicoid peripapillary chorioretinal degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007176", 
            "name": "peripapillary chorioretinal Degeneration, Icelandic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007176", 
            "name": "SVEINSSON chorioretinal atrophy; SCRA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007176", 
            "name": "SCRA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007176", 
            "name": "atrophia areata"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007176", 
            "name": "helicoidal peripapillary chorioretinal Degeneration"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111228", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111228", 
            "name": "HPCD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111228", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111228", 
            "name": "SCRA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111228", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111228", 
            "name": "atrophia areata"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111228", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111228", 
            "name": "helicoid peripapillary chorioretinal degeneration"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111228", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111228", 
            "name": "peripapillary chorioretinal degeneration, Icelandic type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111228", 
        "description": "An eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that has_material_basis_in heterozygous muation in TEAD1 on 11p15.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111228", 
        "name": "Sveinsson chorioretinal atrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111228#disease-associations", 
            "id": "0111228", 
            "database": "Alliance of Genome Resources"
        }
    ]
}