{
  "id": 9426,
  "label": "oculocerebrocutaneous syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008108",
  "properties": {
    "xrefs": [
      "GARD:0000106",
      "ICD9:759.89",
      "MEDGEN:163214",
      "MESH:C538088",
      "NORD:1521",
      "OMIM:164180",
      "Orphanet:1647",
      "SCTID:403554008",
      "UMLS:C0796092"
    ],
    "synonyms": [
      "Delleman syndrome",
      "Delleman-Oorthuys syndrome",
      "Leichtman-Wood-Rohn syndrome",
      "OCCS",
      "oculocerebrocutaneous syndrome",
      "orbital cyst with cerebral and focal dermal malformations",
      "Delleman Oorthuys syndrome",
      "OCC syndrome",
      "oculo-cerebro-cutaneous syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Oculocerebrocutaneous syndrome (OCCS) is a rare congenital disorder associated with an intellectual disability and is typically characterized by the triad of eye, central nervous system and skin malformations."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}