{
  "id": 15791,
  "label": "spasticity-ataxia-gait anomalies syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014803",
  "properties": {
    "xrefs": [
      "GARD:0012681",
      "MEDGEN:905660",
      "OMIM:616859",
      "Orphanet:401866",
      "UMLS:C4225178"
    ],
    "synonyms": [
      "SPAHGC",
      "childhood-onset spasticity with variant non-ketotic hyperglycinemia",
      "spasticity, childhood-onset, with hyperglycinemia",
      "childhood-onset spasticity with hyperglycinemia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18062,
      "label": "spastic ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24045
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050952",
          "GARD:0021401",
          "MEDGEN:376528",
          "MESH:C564815",
          "OMIMPS:108600",
          "Orphanet:316226",
          "UMLS:C1849156"
        ],
        "synonyms": [
          "SPAX"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0017845"
    },
    {
      "id": 18473,
      "label": "inherited lipoic acid biosynthesis defect",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5908,
        22984,
        23517,
        23664
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012679",
          "MEDGEN:1843250",
          "Orphanet:401854",
          "UMLS:C5680006"
        ],
        "synonyms": [
          "inborn error of lipoate biosynthetic process",
          "inborn lipoate biosynthetic process disorder",
          "lipoate biosynthesis defect",
          "rare inborn error of lipoate biosynthetic process",
          "lipoic acid biosynthesis defect",
          "lipoic acid biosynthesis defects"
        ],
        "definition": "An inherited metabolic disease that is has its basis in the disruption of lipoate biosynthetic process."
      },
      "child_count": 24,
      "reference_id": "MONDO:0018424"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18062,
      "label": "spastic ataxia"
    },
    {
      "id": 18473,
      "label": "inherited lipoic acid biosynthesis defect"
    }
  ]
}