{
  "id": 15237,
  "label": "juvenile onset Parkinson disease 19A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014231",
  "properties": {
    "xrefs": [
      "DOID:0060891",
      "GARD:0018461",
      "MEDGEN:816141",
      "OMIM:615528",
      "UMLS:C3809811"
    ],
    "synonyms": [
      "DNAJC6 Parkinson disease",
      "Parkinson disease caused by mutation in DNAJC6",
      "juvenile onset Parkinson disease 19A",
      "juvenile onset Parkinson disease type 19A",
      "PARK19",
      "PARK19A",
      "Park19, formerly",
      "Parkinson disease 19, juvenile-onset",
      "Parkinson disease 19A, juvenile-onset",
      "Parkinson disease 19B, early-onset",
      "juvenile onset Parkinson's disease 19A"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any Parkinson disease in which the cause of the disease is a mutation in the DNAJC6 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3149,
      "label": "juvenile-onset Parkinson disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17603
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060893",
          "GARD:0022833",
          "MEDGEN:155699",
          "UMLS:C0752105"
        ],
        "synonyms": [
          "juvenile-onset Parkinson's disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0000828"
    },
    {
      "id": 18416,
      "label": "atypical juvenile parkinsonism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20335
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017621",
          "MEDGEN:1380105",
          "Orphanet:391411",
          "SCTID:725146001",
          "UMLS:C4510873"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Atypical juvenile parkinsonism (AJP) is a complex form of young-onset Parkinson disease (YOPD) that manifests with pyramidal signs, eye movement abnormalities, psychiatric manifestations (depression, anxiety, drug-induced psychosis, and impulse control disorders), intellectual disability, and other neurological symptoms (such as ataxia and epilepsy) along with classical parkinsonian symptoms."
      },
      "child_count": 1,
      "reference_id": "MONDO:0018321"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3149,
      "label": "juvenile-onset Parkinson disease"
    },
    {
      "id": 18416,
      "label": "atypical juvenile parkinsonism"
    }
  ]
}