{
  "id": 12341,
  "label": "Parkinson disease 3, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011220",
  "properties": {
    "xrefs": [
      "DOID:0111250",
      "GARD:0008578",
      "MEDGEN:355499",
      "MESH:C566552",
      "OMIM:602404",
      "UMLS:C1865581"
    ],
    "synonyms": [
      "PARK3",
      "Parkinson disease 3, autosomal dominant",
      "Parkinson disease 3, autosomal dominant Lewy body",
      "Parkinson disease type 3",
      "autosomal dominant Parkinson disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17603,
      "label": "young-onset Parkinson disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6901
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060894",
          "GARD:0016610",
          "MEDGEN:907947",
          "Orphanet:2828",
          "SCTID:715345007",
          "UMLS:C4275179"
        ],
        "synonyms": [
          "YOPD",
          "early-onset Parkinson disease",
          "early-onset Parkinson's disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A form of Parkinson disease (PD) characterized by an age of onset between 21-45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints and falls, and other non-motor symptoms. A slow disease progression and a more pronounced response to dopaminergic therapy are also observed in most YOPD forms."
      },
      "child_count": 9,
      "reference_id": "MONDO:0017279"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17603,
      "label": "young-onset Parkinson disease"
    }
  ]
}