{
  "id": 14275,
  "label": "hereditary spastic paraplegia 41",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013239",
  "properties": {
    "xrefs": [
      "DOID:0110793",
      "GARD:0017471",
      "MEDGEN:854815",
      "OMIM:613364",
      "Orphanet:320355",
      "SCTID:763069002",
      "UMLS:C3888208"
    ],
    "synonyms": [
      "SPG41",
      "autosomal dominant spastic paraplegia type 41",
      "hereditary spastic paraplegia type 41",
      "spastic paraplegia 41, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Autosomal dominant spastic paraplegia type 41 is a pure form of hereditary spastic paraplegia characterized by onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16081,
      "label": "pure hereditary spastic paraplegia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18959
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019822",
          "MEDGEN:581445",
          "NANDO:1200053",
          "Orphanet:102012",
          "SCTID:230260007",
          "UMLS:C0393555"
        ],
        "synonyms": [
          "Pure HSP",
          "Pure SPG",
          "Pure familial spastic paraplegia",
          "uncomplicated HSP",
          "uncomplicated SPG",
          "uncomplicated familial spastic paraplegia",
          "uncomplicated hereditary spastic paraplegia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 12,
      "reference_id": "MONDO:0015149"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16081,
      "label": "pure hereditary spastic paraplegia"
    }
  ]
}