{
  "id": 15870,
  "label": "striatonigral degeneration, childhood-onset",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014889",
  "properties": {
    "xrefs": [
      "GARD:0017918",
      "MEDGEN:934710",
      "OMIM:617054",
      "Orphanet:497906",
      "UMLS:C4310743"
    ],
    "synonyms": [
      "Lenk-Ploski syndrome",
      "SNDC",
      "childhood-onset basal ganglia degeneration syndrome",
      "striatonigral Degeneration, childhood-onset",
      "striatonigral degeneration, childhood-onset; SNDC"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5100,
      "label": "striatonigral degeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        9146,
        18954,
        21292
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4751",
          "GARD:0023374",
          "ICD10CM:G23.2",
          "ICD9:333.0",
          "MEDGEN:124366",
          "MESH:D020955",
          "NCIT:C125695",
          "OMIMPS:271930",
          "SCTID:29618004",
          "UMLS:C0270733",
          "icd11.foundation:195535779"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements."
      },
      "child_count": 9,
      "reference_id": "MONDO:0003122"
    },
    {
      "id": 23452,
      "label": "inherited dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021630",
          "MEDGEN:1842468",
          "NANDO:1200511",
          "NCIT:C35527",
          "OMIMPS:128100",
          "Orphanet:391799",
          "UMLS:C5680022"
        ],
        "synonyms": [
          "familial dystonia",
          "hereditary dystonic disorder",
          "rare genetic dystonia",
          "rare genetic dystonic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of dystonic disorder that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 48,
      "reference_id": "MONDO:0044807"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5100,
      "label": "striatonigral degeneration"
    },
    {
      "id": 23452,
      "label": "inherited dystonia"
    }
  ]
}