{
  "id": 26613,
  "label": "KY-related neuromyopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:1010194",
  "properties": {
    "synonyms": [
      "KY-related neuromyopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any neuromyopathy in which the cause of the disease is mutation in the KY gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 24271,
      "label": "hereditary neuromuscular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18957,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026275"
        ],
        "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 that is characterized by progressive muscle degeneration and weakness."
      },
      "child_count": 44,
      "reference_id": "MONDO:0100546"
    }
  ],
  "children": [
    {
      "id": 15901,
      "label": "myofibrillar myopathy 7",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        18865,
        26613
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080098",
          "GARD:0025034",
          "MEDGEN:934678",
          "OMIM:617114",
          "UMLS:C4310711"
        ],
        "synonyms": [
          "KY myofibrillar myopathy (disease)",
          "alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathy",
          "myofibrillar myopathy (disease) caused by mutation in KY",
          "myopathy, myofibrillar, 7",
          "myopathy, myofibrillar, type 7",
          "MFM7"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any myofibrillar myopathy in which the cause of the disease is a mutation in the KY gene."
      },
      "child_count": 3,
      "reference_id": "MONDO:0014922"
    },
    {
      "id": 23379,
      "label": "kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16082,
        26613
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022012",
          "MEDGEN:1798875",
          "Orphanet:496689",
          "UMLS:C5567452"
        ],
        "synonyms": [
          "kyphoscoliosis-lateral tongue atrophy-HSP syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0044648"
    }
  ],
  "roots": [
    {
      "id": 24271,
      "label": "hereditary neuromuscular disease"
    }
  ]
}