{
  "id": 18378,
  "label": "familial syringomyelia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018257",
  "properties": {
    "xrefs": [
      "GARD:0021589",
      "MEDGEN:1842994",
      "Orphanet:370034",
      "UMLS:C5680970"
    ],
    "synonyms": [
      "hereditary syringomyelia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An instance of syringomyelia that is caused by an inherited modification of the individual's genome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19959,
      "label": "primary syringomyelia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18163
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019691",
          "MEDGEN:721465",
          "Orphanet:99856",
          "SCTID:371076006",
          "UMLS:C1299627",
          "icd11.foundation:257905685"
        ],
        "synonyms": [
          "congenital syringomyelia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0020508"
    },
    {
      "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": 19959,
      "label": "primary syringomyelia"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}