{
  "id": 18640,
  "label": "autosomal dominant complex spastic paraplegia type 9B",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018644",
  "properties": {
    "xrefs": [
      "GARD:0021866",
      "MEDGEN:1800402",
      "Orphanet:447757",
      "UMLS:C5568979"
    ],
    "synonyms": [
      "AD-SPG9B"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16057,
      "label": "autosomal dominant spastic paraplegia type 9",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16056,
        23875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025059",
          "MEDGEN:322007",
          "Orphanet:100990",
          "UMLS:C1832669",
          "icd11.foundation:1867328407"
        ],
        "synonyms": [
          "ALDH18A1 autosomal dominant complex spastic paraplegia",
          "SPG9",
          "autosomal dominant complex spastic paraplegia caused by mutation in ALDH18A1",
          "cataracts-motor neuropathy-short stature-skeletal anomalies syndrome",
          "spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome",
          "autosomal dominant spastic paraparesis",
          "bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy",
          "cataracts, motor neuronopathy, short stature and skeletal abnormalities",
          "spastic paraplegia 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal dominant complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene."
      },
      "child_count": 4,
      "reference_id": "MONDO:0015091"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16057,
      "label": "autosomal dominant spastic paraplegia type 9"
    }
  ]
}