{
  "id": 26296,
  "label": "juvenile neuronal ceroid lipofuscinosis 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0979346",
  "properties": {
    "xrefs": [
      "Orphanet:699780"
    ],
    "synonyms": [
      "juvenile CLN3 disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10039,
      "label": "neuronal ceroid lipofuscinosis 3",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16851
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110731",
          "GARD:0005897",
          "MEDGEN:155549",
          "NCIT:C61258",
          "NORD:843",
          "OMIM:204200",
          "Orphanet:228346",
          "UMLS:C0751383"
        ],
        "synonyms": [
          "CLN3",
          "CLN3 neuronal ceroid lipofuscinosis",
          "Juvenile CLN3 Disease",
          "ceroid lipofuscinosis, neuronal, type 3",
          "neuronal ceroid lipofuscinosis 3",
          "neuronal ceroid lipofuscinosis caused by mutation in CLN3",
          "neuronal ceroid lipofuscinosis type 3",
          "CLN3 disease",
          "CLN3 disease, juvenile",
          "Spielmeyer Sjogren disease",
          "Spielmeyer-Sjogren disease",
          "Vogt Spielmeyer disease",
          "Vogt-Spielmeyer disease",
          "batten disease",
          "ceroid lipofuscinosis, neuronal, 3",
          "neuronal ceroid lipofuscinosis, juvenile"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments."
      },
      "child_count": 2,
      "reference_id": "MONDO:0008767"
    },
    {
      "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": 10039,
      "label": "neuronal ceroid lipofuscinosis 3"
    },
    {
      "id": 19123,
      "label": "juvenile neuronal ceroid lipofuscinosis"
    }
  ]
}