{
    "disease_id": "DOID:0110373", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013610", 
            "name": "RP61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013610", 
            "name": "retinitis pigmentosa caused by mutation in CLRN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013610", 
            "name": "retinitis pigmentosa type 61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013610", 
            "name": "retinitis pigmentosa 61; RP61"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013610", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013610", 
            "name": "CLRN1 retinitis pigmentosa"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110373", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110373", 
            "name": "RP61"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110373", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the CLRN1 gene on chromosome 3q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110373", 
        "name": "retinitis pigmentosa 61"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614180", 
            "id": "614180", 
            "database": "MIM"
        }
    ]
}