{
  "id": 26312,
  "label": "late infantile neuronal ceroid lipofuscinosis 8",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0979370",
  "properties": {
    "xrefs": [
      "Orphanet:700484"
    ],
    "synonyms": [
      "late infantile CLN8 disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11966,
      "label": "neuronal ceroid lipofuscinosis 8",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16851
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110723",
          "GARD:0017152",
          "MEDGEN:374004",
          "MESH:C537952",
          "OMIM:600143",
          "Orphanet:228354",
          "SCTID:703526007",
          "UMLS:C1838570"
        ],
        "synonyms": [
          "CLN8",
          "CLN8 neuronal ceroid lipofuscinosis",
          "ceroid lipofuscinosis, neuronal, type 8",
          "neuronal ceroid lipofuscinosis 8",
          "neuronal ceroid lipofuscinosis caused by mutation in CLN8",
          "neuronal ceroid lipofuscinosis type 8",
          "CLN8 disease",
          "ceroid lipofuscinosis, neuronal, 8"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the CLN8 gene."
      },
      "child_count": 2,
      "reference_id": "MONDO:0010830"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11966,
      "label": "neuronal ceroid lipofuscinosis 8"
    }
  ]
}