{
  "id": 12132,
  "label": "hereditary spastic paraplegia 9A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011006",
  "properties": {
    "xrefs": [
      "DOID:0110824",
      "GARD:0009583",
      "MEDGEN:1800401",
      "MESH:C536868",
      "OMIM:601162",
      "Orphanet:447753",
      "UMLS:C5568978"
    ],
    "synonyms": [
      "AD-SPG9A",
      "SPG9A",
      "hereditary spastic paraplegia type 9A",
      "cataracts with motor neuronopathy, short stature, and skeletal abnormalities",
      "spastic paraparesis with amyopathy, cataracts, and gastroesophageal reflux",
      "spastic paraparesis with amyotrophy, cataracts, and gastroesophageal reflux",
      "spastic paraplegia 9A, autosomal dominant"
    ],
    "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"
    }
  ]
}