{
  "id": 9704,
  "label": "neurogenic scapuloperoneal syndrome, Kaeser type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008407",
  "properties": {
    "xrefs": [
      "DOID:0111551",
      "GARD:0010312",
      "MEDGEN:356670",
      "MESH:C566695",
      "OMIM:181400",
      "Orphanet:85146",
      "UMLS:C1867005"
    ],
    "synonyms": [
      "Kaeser syndrome",
      "stark-Kaeser syndrome",
      "SCPNK",
      "scapuloperoneal syndrome, neurogenic type, of Kaeser",
      "scapuloperoneal syndrome, neurogenic, Kaeser type"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16774,
      "label": "qualitative or quantitative defects of desmin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16773,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020426",
          "MEDGEN:1842905",
          "Orphanet:209041",
          "UMLS:C5680839"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 10,
      "reference_id": "MONDO:0016187"
    },
    {
      "id": 21302,
      "label": "hereditary motor neuron disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19749,
        21292,
        24271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019478",
          "MEDGEN:78728",
          "Orphanet:98505",
          "SCTID:49793008",
          "UMLS:C0270763"
        ],
        "synonyms": [
          "genetic anterior horn cell disease",
          "genetic motor neuron disease",
          "hereditary motor neuron disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of motor neuron disease that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 27,
      "reference_id": "MONDO:0024257"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16774,
      "label": "qualitative or quantitative defects of desmin"
    },
    {
      "id": 21302,
      "label": "hereditary motor neuron disease"
    }
  ]
}