{
  "id": 25950,
  "label": "intermediate collagen VI-related muscular dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958353",
  "properties": {
    "xrefs": [
      "GARD:0027027",
      "MEDGEN:1853152",
      "Orphanet:646113",
      "UMLS:C5816698"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A form of congenital muscular dystrophy characterized by congenital weakness, hypotonia, proximal joint contractures, marked hyperlaxity of the distal joints, attainment of independent ambulation which is subsequently lost and uniform respiratory insufficiency during the teenage years."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25811,
      "label": "collagen 6-related congenital muscular dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19667
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026920",
          "MEDGEN:1864182",
          "Orphanet:646098",
          "UMLS:C5816703"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0958077"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25811,
      "label": "collagen 6-related congenital muscular dystrophy"
    }
  ]
}