{
    "disease_id": "DOID:0110390", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "RP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "retinitis pigmentosa 1; RP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "retinitis pigmentosa; RP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "retinitis pigmentosa caused by mutation in RP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "RP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "RP1 retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008377", 
            "name": "retinitis pigmentosa type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110390", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110390", 
            "name": "RP1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110390", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the RP1 gene on chromosome 8q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110390", 
        "name": "retinitis pigmentosa 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110390#disease-associations", 
            "id": "0110390", 
            "database": "Alliance of Genome Resources"
        }
    ]
}