{
  "id": 22354,
  "label": "lissencephaly 9 with complex brainstem malformation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0032677",
  "properties": {
    "xrefs": [
      "DOID:0112228",
      "GARD:0018007",
      "MEDGEN:1681109",
      "OMIM:618325",
      "Orphanet:572013",
      "UMLS:C5193029"
    ],
    "synonyms": [
      "LIS9",
      "LISSENCEPHALY 9 WITH COMPLEX BRAINSTEM MALFORMATION"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24198,
      "label": "lissencephaly spectrum disorder with complex brainstem malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18774
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026233"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A lissencephaly spectrum disorder that manifests as posterior predominant pachygyria (ranging from mild severity to classic lissencephaly) and brainstem malformations which include brainstem dysplasia (typically with reduced anteroposterior thickness and transverse broadening of the pons/medulla) and midline crossing defects (anterior commissure, transverse pontine fibers, pyramidal tract, callosum hypoplasia)."
      },
      "child_count": 1,
      "reference_id": "MONDO:0100472"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24198,
      "label": "lissencephaly spectrum disorder with complex brainstem malformation"
    }
  ]
}