{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "RP with or without Pprpe"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "RP12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "RP 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "retinitis pigmentosa with or without Paraarteriolar preservation of retinal pigment epithelium"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "retinitis pigmentosa type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "RP with or without preserved Paraarteriole retinal pigment epithelium"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "retinitis pigmentosa 12; RP12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "CRB1 retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010818", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010818", 
            "name": "retinitis pigmentosa caused by mutation in CRB1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110358", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110358", 
            "name": "RP12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110358", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the CRB1 gene on chromosome 1q31.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110358", 
        "name": "retinitis pigmentosa 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600105", 
            "id": "600105", 
            "database": "MIM"
        }
    ]
}