{
  "id": 18030,
  "label": "parkinsonism due to ATP13A2 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017809",
  "properties": {
    "xrefs": [
      "GARD:0017427",
      "MEDGEN:1687881",
      "Orphanet:314632",
      "SCTID:789657008",
      "UMLS:C5230619"
    ],
    "synonyms": [
      "CLN12 disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 12794,
      "label": "Kufor-Rakeb syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3149,
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060556",
          "GARD:0009174",
          "MEDGEN:338281",
          "MESH:C537177",
          "NORD:1959",
          "OMIM:606693",
          "Orphanet:306674",
          "UMLS:C1847640"
        ],
        "synonyms": [
          "Kufor Rakeb Syndrome",
          "Kufor-Rakeb syndrome",
          "PARK9",
          "KRPPD",
          "KRS",
          "Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia",
          "Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia",
          "Parkinson disease 9, autosomal recessive",
          "Parkinson disease 9, autosomal recessive, juvenile-onset",
          "Parkinson disease type 9",
          "ceroid lipofuscinosis, neuronal, 12",
          "park 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment."
      },
      "child_count": 2,
      "reference_id": "MONDO:0011706"
    },
    {
      "id": 19123,
      "label": "juvenile neuronal ceroid lipofuscinosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16851,
        19753
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050756",
          "GARD:0004938",
          "MedDRA:10052073",
          "NANDO:1200154",
          "NANDO:2201243",
          "Orphanet:79264",
          "SCTID:61663001",
          "icd11.foundation:1716107919"
        ],
        "synonyms": [
          "JNCL",
          "Spielmeyer-Vogt disease",
          "batten disease",
          "juvenile NCL",
          "juvenile neuronal ceroid lipofuscinosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterized by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities."
      },
      "child_count": 16,
      "reference_id": "MONDO:0019262"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 12794,
      "label": "Kufor-Rakeb syndrome"
    },
    {
      "id": 19123,
      "label": "juvenile neuronal ceroid lipofuscinosis"
    }
  ]
}