{
    "disease_id": "DOID:0070486",
    "recommended_name": {
        "id": "DOID:0070486",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070486",
        "name": "Parkinson's disease 25",
        "description": "An early-onset Parkinson's disease characterized by mild to moderately impaired intellectual development that has_material_basis_in homozygous or compound heterozygous mutation in the PTPA gene on chromosome 9q34.11."
    },
    "synonyms": [
        {
            "id": "DOID:0070486",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070486",
            "name": "autosomal recessive early-onset Parkinson disease 25 with impaired intellectual development",
            "description": ""
        },
        {
            "id": "DOID:0070486",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070486",
            "name": "PARK25",
            "description": ""
        },
        {
            "id": "MONDO:0957576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957576",
            "name": "parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development",
            "description": ""
        }
    ]
}