{
    "disease_id": "DOID:0110376", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012796", 
            "name": "retinitis pigmentosa 41; RP41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012796", 
            "name": "RP 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012796", 
            "name": "retinitis pigmentosa type 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012796", 
            "name": "PROM1 retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012796", 
            "name": "retinal Degeneration, autosomal recessive, prominin-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012796", 
            "name": "retinitis pigmentosa caused by mutation in PROM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012796", 
            "name": "RP41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110376", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110376", 
            "name": "RP41"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110376", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110376", 
        "name": "retinitis pigmentosa 41"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612095", 
            "id": "612095", 
            "database": "MIM"
        }
    ]
}