{
    "disease_id": "DOID:0110409", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110409", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110409", 
            "name": "RP46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the IDH3B gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "retinitis pigmentosa 46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "RP46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "retinitis pigmentosa caused by mutation in IDH3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "retinitis pigmentosa 46; RP46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "retinitis pigmentosa, autosomal recessive, Idh3B-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "retinitis pigmentosa 46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "retinitis pigmentosa type 46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012943", 
            "name": "IDH3B retinitis pigmentosa"
        }, 
        {
            "url": "https://www.omim.org/entry/612572", 
            "description": "Retinitis pigmentosa 46", 
            "resource": "MIM", 
            "id": "MIM:612572", 
            "name": "Retinitis pigmentosa 46"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110409", 
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the IDH3B on chromosome 20p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110409", 
        "name": "retinitis pigmentosa 46"
    }
}