{
  "id": 20835,
  "label": "corticobasal degeneration disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022308",
  "properties": {
    "xrefs": [
      "GARD:0000046",
      "ICD10CM:G31.85",
      "MEDGEN:95979",
      "NANDO:1200011",
      "NCIT:C129069",
      "SCTID:18842008",
      "UMLS:C0393570"
    ],
    "synonyms": [
      "cortical basal ganglionic degeneration",
      "corticobasal degeneration",
      "CBGD",
      "cortical-basal ganglionic degeneration",
      "cortico-basal ganglionic Degeneration (CBGD)",
      "corticobasal syndrome",
      "corticodentatonigral degeneration with neuronal achromasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A progressive neurodegenerative condition affecting the cerebral cortex and basal ganglia. The disorder is characterized by varying degrees of cognitive and motor impairment."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 21293,
      "label": "cerebral degeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208,
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:331.9",
          "MEDGEN:56343",
          "SCTID:418143002",
          "UMLS:C0154671"
        ],
        "synonyms": [
          "cerebral degeneration",
          "neurodegenerative disease of telencephalon",
          "telencephalon neurodegenerative disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodegenerative disease that involves the telencephalon."
      },
      "child_count": 4,
      "reference_id": "MONDO:0024238"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 21293,
      "label": "cerebral degeneration"
    }
  ]
}