{
  "id": 22078,
  "label": "COACH syndrome 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0030862",
  "properties": {
    "xrefs": [
      "GARD:0016423",
      "MEDGEN:1755565",
      "OMIM:619113",
      "UMLS:C5436841"
    ],
    "synonyms": [
      "COACH3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24077,
      "label": "COACH syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16225,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111589",
          "GARD:0001410",
          "MEDGEN:387879",
          "MESH:C536430",
          "Orphanet:1454",
          "SCTID:721847002",
          "UMLS:C1857662"
        ],
        "synonyms": [
          "JS-H",
          "Joubert syndrome with congenital hepatic fibrosis",
          "Joubert syndrome with hepatic defect",
          "cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis",
          "gentile syndrome",
          "cerebellar vermis hypo/aplasia, oligophrenia, ataxia congenital, coloboma, and hepatic fibrosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A Mendelian disease characterized by infantile ataxia with hypo/aplastic vermis, hepatic fibrocirrhosis, slender-shaped skeleton, peculiar face, and moderate intellectual disability."
      },
      "child_count": 6,
      "reference_id": "MONDO:0100349"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24077,
      "label": "COACH syndrome"
    }
  ]
}