{
  "id": 15844,
  "label": "cerebral palsy, spastic quadriplegic, 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014862",
  "properties": {
    "xrefs": [
      "DOID:0081361",
      "GARD:0018310",
      "MEDGEN:934734",
      "OMIM:617008",
      "UMLS:C4310767"
    ],
    "synonyms": [
      "ADD3 spastic quadriplegia",
      "CPSQ3",
      "cerebral palsy, spastic quadriplegic, 3",
      "cerebral palsy, spastic quadriplegic, 3; CPSQ3",
      "cerebral palsy, spastic quadriplegic, type 3",
      "spastic quadriplegia caused by mutation in ADD3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any spastic quadriplegia in which the cause of the disease is a mutation in the ADD3 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16798,
      "label": "spastic quadriplegic cerebral palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2891,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10970",
          "GARD:0017109",
          "ICD10CM:G80.0",
          "ICD9:343.2",
          "ICD9:344.09",
          "MEDGEN:98433",
          "NCIT:C116904",
          "OMIMPS:603513",
          "OMIMPS:612900",
          "Orphanet:210141",
          "SCTID:192965001",
          "UMLS:C0426970",
          "icd11.foundation:1155284708"
        ],
        "synonyms": [
          "inherited congenital spastic quadriplegia",
          "quadriplegic infantile cerebral palsy",
          "spastic quadriplegia",
          "spastic quadriplegic cerebral palsy",
          "spastic tetraplegia cerebral palsy",
          "tetraplegic infantile cerebral palsy",
          "inherited congenital spastic tetraplegia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A type of spastic cerebral palsy characterized by increased muscle tone of all four extremities."
      },
      "child_count": 6,
      "reference_id": "MONDO:0016215"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24488
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 550,
      "reference_id": "MONDO:0100500"
    },
    {
      "id": 24241,
      "label": "complex neurodevelopmental disorder with motor features",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23791
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027067"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A complex neurodevelopmental disorder that involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy). Additionally, the disorder features at least one phenotype associated with motor function, including but not limited to spasticity, hypo- or hypertonia, dyskinesia, choreo-athetosis, or ataxia."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100516"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16798,
      "label": "spastic quadriplegic cerebral palsy"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder"
    },
    {
      "id": 24241,
      "label": "complex neurodevelopmental disorder with motor features"
    }
  ]
}