{
  "id": 25510,
  "label": "epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859390",
  "properties": {
    "xrefs": [
      "GARD:0026729",
      "OMIMPS:300491"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 16437,
      "label": "monogenic epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6761
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020086",
          "MEDGEN:1842675",
          "Orphanet:166472",
          "UMLS:C5680430"
        ],
        "synonyms": [
          "monogenic disease with epilepsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 18,
      "reference_id": "MONDO:0015653"
    },
    {
      "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": [
    {
      "id": 11508,
      "label": "epilepsy, X-linked 1, with variable learning disabilities and behavior disorders",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2902,
        25510
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112122",
          "GARD:0016748",
          "MEDGEN:1823951",
          "MESH:C564505",
          "OMIM:300491",
          "Orphanet:85294",
          "UMLS:C5774177"
        ],
        "synonyms": [
          "X-linked epilepsy-learning disabilities-behavior disorders syndrome",
          "epilepsy, X-linked, with variable learning disabilities and behavior disorders, X-linked recessive, X-linked dominant",
          "epilepsy, X-linked, with variable learning disabilities and behaviour disorders, X-linked recessive, X-linked dominant",
          "epilepsy, X-linked, with variable learning disabilities and behavior disorders",
          "epilepsy, X-linked, with variable learning disabilities and behaviour disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features characterized by epilepsy, learning difficulties, macrocephaly, and aggressive behavior. It has been described in males from a four-generation kindred. It is transmitted as an X-linked recessive trait and is likely to be caused by mutations in the gene encoding synapsin I (Xp11.3-q12)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010339"
    },
    {
      "id": 25533,
      "label": "epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25510
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026742",
          "MEDGEN:1823952",
          "OMIM:301091",
          "UMLS:C5774178"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859564"
    }
  ],
  "roots": [
    {
      "id": 16437,
      "label": "monogenic epilepsy"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}