{
  "id": 11912,
  "label": "striatonigral degeneration, infantile, mitochondrial",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010774",
  "properties": {
    "xrefs": [
      "GARD:0018315",
      "MEDGEN:374113",
      "MESH:C564025",
      "OMIM:500003",
      "UMLS:C1839022"
    ],
    "synonyms": [
      "striatonigral degeneration, infantile, mitochondrial",
      "bilateral striatal Necrosis, infantile, mitochondrial",
      "infantile bilateral striatal Necrosis, mitochondrial"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11268,
      "label": "familial infantile bilateral striatal necrosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5100,
        16334
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017141",
          "MEDGEN:1672478",
          "OMIM:271930",
          "Orphanet:225154",
          "UMLS:C4087174",
          "icd11.foundation:1873983370"
        ],
        "synonyms": [
          "familial IBSN",
          "familial infantile striatonigral degeneration",
          "familial infantile striatonigral necrosis",
          "hereditary infantile bilateral striatal necrosis",
          "FBSN",
          "SNDI",
          "bilateral striatal Necrosis, infantile",
          "familial bilateral striatal necrosis",
          "infantile bilateral striatal necrosis",
          "striatal degeneration, familial",
          "striatonigral degeneration, infantile"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "The familial form of infantile bilateral striatal necrosis (IBSN), a syndrome of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis."
      },
      "child_count": 3,
      "reference_id": "MONDO:0010080"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11268,
      "label": "familial infantile bilateral striatal necrosis"
    }
  ]
}