{
  "id": 12550,
  "label": "hereditary spastic paraplegia 11",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011445",
  "properties": {
    "xrefs": [
      "DOID:0110764",
      "GARD:0004919",
      "MEDGEN:388073",
      "NCIT:C148317",
      "OMIM:604360",
      "Orphanet:2822",
      "SCTID:715491000",
      "UMLS:C1858479"
    ],
    "synonyms": [
      "HSP-TCC",
      "Nakamura-Osame syndrome",
      "SPG11",
      "SPG11 hereditary spastic paraplegia",
      "autosomal recessive spastic paraplegia type 11",
      "hereditary spastic paraplegia caused by mutation in SPG11",
      "hereditary spastic paraplegia type 11",
      "spastic paraplegia-intellectual disability-thin corpus callosum syndrome",
      "Nakamura Osame syndrome",
      "hereditary spastic paraplegia mental impairment and thin corpus callosum",
      "spastic paraplegia - intellectual deficit - thin corpus callosum",
      "spastic paraplegia 11",
      "spastic paraplegia 11, autosomal recessive",
      "spastic paraplegia, autosomal recessive, complicated, with thin corpus callosum",
      "spastic paraplegia, autosomal recessive, with mental impairment and thin corpus callosum"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16082,
      "label": "complex hereditary spastic paraplegia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        18959
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019823",
          "MEDGEN:581446",
          "NANDO:1200054",
          "Orphanet:102013",
          "SCTID:230261006",
          "UMLS:C0393556"
        ],
        "synonyms": [
          "Complex HSP",
          "Complex SPG",
          "Complex familial spastic paraplegia",
          "complicated HSP",
          "complicated SPG",
          "complicated familial spastic paraplegia",
          "complicated hereditary spastic paraplegia",
          "syndrome associated with hereditary spastic paraplegia",
          "syndromic hereditary spastic paraplegia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A hereditary spastic paraplegia that is part of a larger syndrome."
      },
      "child_count": 100,
      "reference_id": "MONDO:0015150"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16082,
      "label": "complex hereditary spastic paraplegia"
    }
  ]
}