{
    "disease_id": "DOID:0111541", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008246", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008246", 
            "name": "pigmented paravenous retinochoroidal atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008246", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008246", 
            "name": "PPCRA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008246", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008246", 
            "name": "pigmented paravenous chorioretinal atrophy; PPCRA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008246", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008246", 
            "name": "PPRCA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111541", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111541", 
            "name": "PPRCA"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111541", 
        "description": "An eye disease characterized by the presence of bone corpuscle pigmentation in a paravenous distribution in the ocular fundus that has_material_basis_in heterozygous mutation in CRB1 on chromosome 1q31.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111541", 
        "name": "pigmented paravenous chorioretinal atrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/172870", 
            "id": "172870", 
            "database": "MIM"
        }
    ]
}