{
  "id": 16794,
  "label": "alternating hemiplegia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016210",
  "properties": {
    "xrefs": [
      "GARD:0020446",
      "MEDGEN:124456",
      "Orphanet:209978",
      "SCTID:404689008",
      "UMLS:C0278110",
      "icd11.foundation:774373615"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 24488,
      "label": "neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0010642",
          "MEDGEN:453059",
          "MESH:D065886",
          "MedDRA:10064062",
          "NCIT:C89338",
          "SCTID:700364009",
          "UMLS:C1535926"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A behavioral and cognitive disorder with onset during the developmental period that involves impaired or aberrant development of intellectual, motor, or social functions."
      },
      "child_count": 18,
      "reference_id": "MONDO:0700092"
    }
  ],
  "children": [
    {
      "id": 16793,
      "label": "benign familial nocturnal alternating hemiplegia of childhood",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16794
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020445",
          "MEDGEN:1668716",
          "Orphanet:209973",
          "UMLS:C4749822",
          "icd11.foundation:447920235"
        ],
        "synonyms": [
          "benign familial nocturnal alternating hemiplegia in childhood",
          "benign nocturnal alternating hemiplegia of childhood"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Benign nocturnal alternating hemiplegia of childhood is a rare neurologic disease characterized by recurrent attacks of nocturnal screaming or crying followed or accompanied by unilateral or sometimes bilateral hemiplegia. Disorder is not associated with neurological or developmental impairments but may be associated with mild behavioral abnormalities."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016209"
    },
    {
      "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": 24488,
      "label": "neurodevelopmental disorder"
    }
  ]
}