{
  "id": 14878,
  "label": "neuronal ceroid lipofuscinosis 11",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013866",
  "properties": {
    "xrefs": [
      "DOID:0110732",
      "GARD:0017426",
      "MEDGEN:761331",
      "OMIM:614706",
      "Orphanet:314629",
      "UMLS:C3539123"
    ],
    "synonyms": [
      "CLN11",
      "GRN neuronal ceroid lipofuscinosis",
      "Grn neuronal ceroid lipofuscinosis",
      "ceroid lipofuscinosis, neuronal, type 11",
      "neuronal ceroid lipofuscinosis caused by mutation in GRN",
      "neuronal ceroid lipofuscinosis caused by mutation in Grn",
      "neuronal ceroid lipofuscinosis type 11",
      "CLN11 disease",
      "ceroid lipofuscinosis, neuronal, 11"
    ],
    "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 GRN gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19121,
      "label": "adult neuronal ceroid lipofuscinosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16851,
        19753
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010973",
          "MEDGEN:7230",
          "NANDO:1200155",
          "NANDO:2201244",
          "NORD:1341",
          "Orphanet:79262",
          "SCTID:62009002",
          "UMLS:C0022797",
          "icd11.foundation:1460031344"
        ],
        "synonyms": [
          "ANCL",
          "Kufs disease",
          "adult NCL",
          "adult neuronal ceroid lipofuscinosis",
          "neuronal ceroid lipofuscinosis of adults",
          "CLN4 disease, adult autosomal dominant",
          "Kuf's disease",
          "neuronal ceroid lipofuscinosis 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) with onset during the third decade of life, characterized by dementia, seizures and loss of motor capacities, and sometimes associated with visual loss caused by retinal degeneration."
      },
      "child_count": 10,
      "reference_id": "MONDO:0019260"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19121,
      "label": "adult neuronal ceroid lipofuscinosis"
    }
  ]
}