{
  "id": 24725,
  "label": "argyrophilic grain disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700351",
  "properties": {
    "xrefs": [
      "MEDGEN:572581",
      "UMLS:C0338460"
    ],
    "synonyms": [
      "AGD"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A tauopathy characterized pathologically by the presence of silver stain positive lesions called argyrophilic grains, oligodendrocytic coiled bodies, and neuronal tau-positive pretangles."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7220,
      "label": "tauopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208,
        29384
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:680",
          "EFO:0005815",
          "MEDGEN:181880",
          "MESH:D024801",
          "UMLS:C0949664"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neurodegenerative disorders involving deposition of abnormal tau protein isoforms (tau proteins) in neurons and glial cells in the brain. Pathological aggregations of tau proteins are associated with mutation of the tau gene on chromosome 17 in patients with alzheimer disease; dementia; parkinsonian disorders; progressive supranuclear palsy (supranuclear palsy, progressive); and corticobasal degeneration."
      },
      "child_count": 4,
      "reference_id": "MONDO:0005574"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7220,
      "label": "tauopathy"
    }
  ]
}