{
  "id": 16546,
  "label": "moderate multiminicore disease with hand involvement",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015793",
  "properties": {
    "xrefs": [
      "GARD:0017078",
      "MEDGEN:396213",
      "Orphanet:178145",
      "UMLS:C1861753"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18870,
      "label": "multiminicore myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16783,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080991",
          "GARD:0016536",
          "MEDGEN:75731",
          "NANDO:1200480",
          "NANDO:2200871",
          "Orphanet:598",
          "SCTID:55133004",
          "UMLS:C0270962"
        ],
        "synonyms": [
          "MmD",
          "multicore disease",
          "multicore myopathy",
          "multiminicore disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy."
      },
      "child_count": 10,
      "reference_id": "MONDO:0018948"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18870,
      "label": "multiminicore myopathy"
    }
  ]
}