{
  "id": 12007,
  "label": "band heterotopia of brain",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010873",
  "properties": {
    "xrefs": [
      "GARD:0002250",
      "MEDGEN:924885",
      "MESH:C563950",
      "OMIM:600348",
      "UMLS:C4284594"
    ],
    "synonyms": [
      "band heterotopia of brain",
      "BH",
      "band heterotopia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19945,
      "label": "subcortical band heterotopia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        4427
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111169",
          "GARD:0001904",
          "MEDGEN:336288",
          "NANDO:1201070",
          "NCIT:C116933",
          "Orphanet:99796",
          "UMLS:C1848201",
          "icd11.foundation:525786944"
        ],
        "synonyms": [
          "double cortex syndrome",
          "subcortical laminar heterotopia",
          "Double cortex",
          "familial band heterotopia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A developmental brain abnormality characterized by atypical migration of neurons during cortical development."
      },
      "child_count": 4,
      "reference_id": "MONDO:0020491"
    },
    {
      "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": 19945,
      "label": "subcortical band heterotopia"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}