{
  "id": 23499,
  "label": "cerebral cortex disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044996",
  "properties": {
    "xrefs": [
      "MEDGEN:688117",
      "SCTID:128128003",
      "UMLS:C1263847"
    ],
    "synonyms": [
      "cerebral cortex disease",
      "cerebral cortex disease or disorder",
      "disease of cerebral cortex",
      "disease or disorder of cerebral cortex",
      "disorder of cerebral cortex"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A disease or disorder that involves the cerebral cortex."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 6,
  "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"
    }
  ],
  "children": [
    {
      "id": 5479,
      "label": "visual cortex disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4014,
        23499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5691",
          "GARD:0027642",
          "ICD10CM:H47.6",
          "ICD9:377.7",
          "MEDGEN:66699",
          "NCIT:C35275",
          "Orphanet:447788",
          "SCTID:128329001",
          "UMLS:C0234398"
        ],
        "synonyms": [
          "disease of visual cortex",
          "disease or disorder of visual cortex",
          "disorder of visual cortex",
          "visual cortex disease",
          "visual cortex disease or disorder",
          "visual cortex disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A disease involving the visual cortex."
      },
      "child_count": 4,
      "reference_id": "MONDO:0003584"
    },
    {
      "id": 6488,
      "label": "occipital lobe neoplasm",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20533,
        23499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:910",
          "ICD10CM:C71.4",
          "ICD9:191.4",
          "MEDGEN:220389",
          "NCIT:C5574",
          "SCTID:126957005",
          "UMLS:C1263889"
        ],
        "synonyms": [
          "malignant neoplasm of occipital lobe",
          "neoplasm of occipital lobe",
          "neoplasm of the occipital lobe",
          "occipital lobe neoplasm",
          "occipital lobe neoplasm (disease)",
          "occipital lobe tumor",
          "occipital lobe tumour",
          "tumor of occipital lobe",
          "tumor of the occipital lobe",
          "tumour of occipital lobe",
          "tumour of the occipital lobe"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neoplasm involving a occipital lobe."
      },
      "child_count": 0,
      "reference_id": "MONDO:0004709"
    },
    {
      "id": 7196,
      "label": "hippocampal sclerosis of aging",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005678",
          "MEDGEN:1801569",
          "UMLS:C5691287"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Age-related neuropathological condition with severe neuronal cell loss and gliosis in the hippocampus"
      },
      "child_count": 0,
      "reference_id": "MONDO:0005544"
    },
    {
      "id": 7991,
      "label": "cerebral palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7990,
        23499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "CSP:0723-4729",
          "DOID:1969",
          "EFO:1000632",
          "HP:0100021",
          "ICD10CM:G80",
          "ICD10WHO:G80",
          "ICD9:343.8",
          "ICD9:343.9",
          "MEDGEN:854",
          "MESH:D002547",
          "NCIT:C34460",
          "SCTID:128188000",
          "UMLS:C0007789",
          "icd11.foundation:76906748"
        ],
        "synonyms": [
          "infantile cerebral palsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of disorders affecting the development of movement and posture, often accompanied by disturbances of sensation, perception, cognition, and behavior. It results from damage to the fetal or infant brain."
      },
      "child_count": 10,
      "reference_id": "MONDO:0006497"
    },
    {
      "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": 23031,
      "label": "primary motor cortex epilepsy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4663,
        23499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:536338",
          "SCTID:267592003",
          "UMLS:C0234978"
        ],
        "synonyms": [
          "epilepsy of primary motor cortex",
          "primary motor cortex epilepsy",
          "Jacksonian epilepsy",
          "motor cortex epilepsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A epilepsy that involves the primary motor cortex."
      },
      "child_count": 0,
      "reference_id": "MONDO:0041284"
    }
  ],
  "roots": [
    {
      "id": 7209,
      "label": "brain disorder"
    }
  ]
}