{
  "id": 21293,
  "label": "cerebral degeneration",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024238",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 7208,
      "label": "neurodegenerative disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1289",
          "EFO:0005772",
          "ICD9:349.89",
          "MEDGEN:17999",
          "MESH:D019636",
          "NCIT:C4802",
          "SCTID:80690008",
          "UMLS:C0027746"
        ],
        "synonyms": [
          "degenerative disease",
          "brain degeneration",
          "central nervous system degenerative disorder",
          "central nervous system neurodegenerative disorder",
          "degenerative disorder of central nervous system",
          "cerebral degeneration disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disorder of the central nervous system characterized by gradual and progressive loss of neural tissue and neurologic function."
      },
      "child_count": 22,
      "reference_id": "MONDO:0005559"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 9550,
      "label": "Pick disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17600,
        21293,
        23499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11870",
          "EFO:0003096",
          "GARD:0024611",
          "ICD10CM:G31.01",
          "ICD9:331.11",
          "MEDGEN:116020",
          "MESH:D020774",
          "NCIT:C85008",
          "OMIM:172700",
          "SCTID:13092008",
          "UMLS:C0236642"
        ],
        "synonyms": [
          "PICK disease of brain",
          "Pick disease",
          "lobar atrophy of brain",
          "Pick disease of the brain",
          "Pick's disease",
          "dementia with lobar atrophy and neuronal cytoplasmic inclusions",
          "lobar atrophy of the brain"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare neurodegenerative disorder leading to dementia. It is characterized by frontotemporal lobar degeneration with accumulation of tau proteins which form Pick bodies."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008243"
    },
    {
      "id": 20835,
      "label": "corticobasal degeneration disorder",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        21293
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0022308"
    }
  ],
  "roots": [
    {
      "id": 7208,
      "label": "neurodegenerative disease"
    },
    {
      "id": 7209,
      "label": "brain disorder"
    }
  ]
}