{
  "id": 3414,
  "label": "hemiplegia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001170",
  "properties": {
    "xrefs": [
      "DOID:10969",
      "EFO:0009453",
      "ICD10WHO:G81",
      "ICD9:343.4",
      "MEDGEN:9196",
      "MESH:D006429",
      "SCTID:1593000",
      "UMLS:C0018991",
      "icd11.foundation:1641958762"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Severe or complete loss of motor function on one side of the body. This condition is usually caused by brain diseases that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, brain stem lesions; cervical spinal cord diseases; peripheral nervous system diseases; and other conditions may manifest as hemiplegia. The term hemiparesis (see paresis) refers to mild to moderate weakness involving one side of the body."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7990,
      "label": "palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000631",
          "ICD10CM:G80-G83",
          "MEDGEN:854494",
          "MESH:D010243",
          "UMLS:C3887651",
          "Wikipedia:Palsy"
        ],
        "synonyms": [
          "Plegia",
          "Plegias"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45)"
      },
      "child_count": 10,
      "reference_id": "MONDO:0006496"
    }
  ],
  "children": [
    {
      "id": 16815,
      "label": "alternating hemiplegia of childhood",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3414,
        16794,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050635",
          "GARD:0000011",
          "MEDGEN:90925",
          "MESH:C536589",
          "NANDO:1200403",
          "NANDO:1200525",
          "NANDO:2100239",
          "NANDO:2200357",
          "NANDO:2200883",
          "NCIT:C35261",
          "NORD:758",
          "OMIMPS:104290",
          "Orphanet:2131",
          "SCTID:230466004",
          "UMLS:C0338488",
          "icd11.foundation:301329822"
        ],
        "synonyms": [
          "AHC",
          "adrenal hypoplasia congenita",
          "alternating hemiplegia of childhood",
          "childhood alternating hemiplegia",
          "congenital adrenal Hypoplasia",
          "congenital adrenal gland hypoplasia",
          "paediatric alternating hemiplegia",
          "pediatric alternating hemiplegia",
          "alternating hemiplegia",
          "alternating hemiplegia syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare neurodevelopmental disorder characterized by recurrent episodes of hemiplegia and paroxysmal disturbances associated with persistent developmental delay and cognitive impairment."
      },
      "child_count": 9,
      "reference_id": "MONDO:0016241"
    }
  ],
  "roots": [
    {
      "id": 7990,
      "label": "palsy"
    }
  ]
}