{
  "id": 12861,
  "label": "Alzheimer disease 8",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011777",
  "properties": {
    "xrefs": [
      "DOID:0110041",
      "GARD:0016512",
      "MEDGEN:375956",
      "MESH:C564622",
      "OMIM:607116",
      "UMLS:C1846735"
    ],
    "synonyms": [
      "AD8",
      "Alzheimer disease 8",
      "Alzheimer disease type 8",
      "Alzheimer's disease 8",
      "Alzheimer's disease type 8",
      "Ad8",
      "Alzheimer disease, familial, 8"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An Alzheimer's disease that is characterized by an associated with variation in the region 20p12.2-q11.21."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16078,
      "label": "early-onset autosomal dominant Alzheimer disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        23839
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012798",
          "Orphanet:1020"
        ],
        "synonyms": [
          "EOFAD",
          "early-onset familial autosomal dominant Alzheimer disease",
          "early-onset, autosomal dominant Alzheimer disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A progressive dementia with reduction of cognitive functions. It presents the same phenotype as sporadic Alzheimer disease (AD) but has an early age of onset, usually before 60 years old."
      },
      "child_count": 28,
      "reference_id": "MONDO:0015140"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16078,
      "label": "early-onset autosomal dominant Alzheimer disease"
    }
  ]
}