{
  "id": 11550,
  "label": "rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010388",
  "properties": {
    "xrefs": [
      "GARD:0018282",
      "MEDGEN:337150",
      "MESH:C564467",
      "OMIM:300643",
      "UMLS:C1845070"
    ],
    "synonyms": [
      "rolandic epilepsy, impaired intellectual development, and speech dyspraxia",
      "rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked",
      "rolandic epilepsy, mental retardation, and speech dyspraxia, X-linked",
      "RESDX",
      "ROLANDIC epilepsy, intellectual disability, and speech dyspraxia, X-linked",
      "ROLANDIC epilepsy, mental retardation, and speech dyspraxia, X-linked"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16387,
      "label": "rolandic epilepsy-speech dyspraxia syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19725
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017002",
          "MEDGEN:1633042",
          "Orphanet:163721",
          "UMLS:C4707308",
          "icd11.foundation:288052868"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed."
      },
      "child_count": 2,
      "reference_id": "MONDO:0015587"
    },
    {
      "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": 16387,
      "label": "rolandic epilepsy-speech dyspraxia syndrome"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}