{
  "id": 2753,
  "label": "encephalopathy, acute, infection-induced",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000166",
  "properties": {
    "xrefs": [
      "OMIMPS:610551"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7209,
      "label": "brain disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:936",
          "EFO:0005774",
          "ICD9:348.3",
          "ICD9:348.30",
          "ICD9:348.8",
          "ICD9:348.9",
          "MEDGEN:14214",
          "MESH:D001927",
          "NCIT:C96413",
          "SCTID:81308009",
          "UMLS:C0006111"
        ],
        "synonyms": [
          "brain disease",
          "brain disease or disorder",
          "disease of brain",
          "disease or disorder of brain",
          "disorder of brain",
          "encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease affecting the brain or part of the brain."
      },
      "child_count": 71,
      "reference_id": "MONDO:0005560"
    },
    {
      "id": 20092,
      "label": "acute disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24492
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:799.89",
          "MEDGEN:1738",
          "MESH:D000208",
          "SCTID:2704003",
          "UMLS:C0001314"
        ],
        "synonyms": [
          "acute disease",
          "acute diseases",
          "disease, acute"
        ],
        "definition": "Disease having a short and relatively severe course."
      },
      "child_count": 119,
      "reference_id": "MONDO:0020683"
    },
    {
      "id": 20718,
      "label": "post-infectious disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:B90-B94",
          "ICD9:139.8",
          "MEDGEN:688819",
          "SCTID:123976001",
          "UMLS:C1264603"
        ],
        "synonyms": [
          "sequela of infectious disorder"
        ],
        "definition": "A disorder that follows infection but is distinct from the infection itself and its usual manifestations."
      },
      "child_count": 14,
      "reference_id": "MONDO:0021669"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 13025,
      "label": "familial acute necrotizing encephalopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2753,
        23939
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011953"
    }
  ],
  "roots": [
    {
      "id": 7209,
      "label": "brain disorder"
    },
    {
      "id": 20092,
      "label": "acute disease"
    },
    {
      "id": 20718,
      "label": "post-infectious disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}