{
  "id": 13025,
  "label": "familial acute necrotizing encephalopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011953",
  "properties": {
    "xrefs": [
      "GARD:0013232",
      "MEDGEN:382634",
      "OMIM:608033",
      "Orphanet:88619",
      "SCTID:723359002",
      "UMLS:C2675556"
    ],
    "synonyms": [
      "ADANE",
      "encephalopathy, acute, infection-induced, 3, susceptibility to",
      "encephalopathy, acute, infection-induced, susceptibility to, type 3",
      "recurrent acute necrotizing encephalopathy",
      "ANE1",
      "IIAE3",
      "Postinfectious acute necrotizing hemorrhagic encephalopathy",
      "acute necrotizing encephalopathy type 1",
      "autosomal dominant acute necrotizing encephalopathy",
      "encephalopathy, acute necrotizing, susceptibility to",
      "encephalopathy, acute, infection-induced, susceptibility to, 3",
      "infection-induced acute encephalopathy 3",
      "susceptibility to acute infection-induced encephalopathy-3",
      "susceptibility to acute necrotizing encephalopathy",
      "susceptibility to infection-induced acute encephalopathy 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Familial acute necrotizing encephalopathy or ADANE is a potentially fatal neurological disease characterized by neuropathological lesions principally involving the brainstem, thalamus and putamen."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2753,
      "label": "encephalopathy, acute, infection-induced",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209,
        20092,
        20718,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIMPS:610551"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0000166"
    },
    {
      "id": 23939,
      "label": "Mendelian encephalopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "definition": "An instance of encephalopathy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 19,
      "reference_id": "MONDO:0100198"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2753,
      "label": "encephalopathy, acute, infection-induced"
    },
    {
      "id": 23939,
      "label": "Mendelian encephalopathy"
    }
  ]
}