{
  "id": 10598,
  "label": "normal pressure hydrocephalus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009366",
  "properties": {
    "xrefs": [
      "DOID:1572",
      "EFO:1001065",
      "ICD9:331.5",
      "MEDGEN:42526",
      "MESH:D006850",
      "MedDRA:10029773",
      "OMIM:236690",
      "Orphanet:314928",
      "SCTID:30753002",
      "UMLS:C0020258"
    ],
    "synonyms": [
      "NPH",
      "chronic adult hydrocephalus",
      "hydrocephalus, normal pressure, 1",
      "hydrocephalus, normal-pressure"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see gait disorders, neurologic), progressive intellectual decline, and urinary incontinence. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of csf including subarachnoid hemorrhage, chronic meningitis, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3)"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4192,
      "label": "communicating hydrocephalus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3395
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1573",
          "ICD10CM:G91.0",
          "ICD9:331.3",
          "MEDGEN:1058",
          "NCIT:C34501",
          "SCTID:271569006",
          "UMLS:C0009451",
          "icd11.foundation:186577228"
        ],
        "synonyms": [
          "non-obstructive hydrocephalus"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of impaired cerebrospinal fluid reabsorption by the arachnoid granulations."
      },
      "child_count": 1,
      "reference_id": "MONDO:0002045"
    },
    {
      "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": [],
  "roots": [
    {
      "id": 4192,
      "label": "communicating hydrocephalus"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}