{
  "id": 12123,
  "label": "supranuclear palsy, progressive, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010997",
  "properties": {
    "xrefs": [
      "GARD:0017182",
      "MEDGEN:1640811",
      "OMIM:601104",
      "Orphanet:240071",
      "UMLS:C4551863"
    ],
    "synonyms": [
      "Steele-Richardson-Olszewski disease",
      "Steele-Richardson-Olszewski syndrome",
      "PSP",
      "Richardson syndrome",
      "classic PSP syndrome",
      "classic progressive supranuclear palsy syndrome",
      "supranuclear palsy, progressive",
      "supranuclear palsy, progressive, 1",
      "supranuclear palsy, progressive, type 1",
      "PSNP1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Classical progressive supranuclear palsy, also known as Richardson's syndrome, is the most common clinical variant of progressive supranuclear palsy (PSP), a rare late-onset neurodegenerative disease characterized by postural instability, progressive rigidity, supranuclear gaze palsy and mild dementia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18949,
      "label": "progressive supranuclear palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        7073,
        19772,
        21292
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:678",
          "GARD:0007471",
          "ICD10CM:G23.1",
          "ICD9:333.0",
          "MEDGEN:21026",
          "MESH:D013494",
          "MedDRA:10036813",
          "NANDO:1200009",
          "NCIT:C85028",
          "NORD:1619",
          "OMIMPS:601104",
          "Orphanet:683",
          "SCTID:192976002",
          "SCTID:28978003",
          "UMLS:C0038868",
          "icd11.foundation:1493396558"
        ],
        "synonyms": [
          "PSP syndrome",
          "Steele-Richardson-Olszewski disease",
          "Steele-Richardson-Olszewski syndrome",
          "progressive supranuclear ophthalmoplegia",
          "familial progressive supranuclear palsy (type)",
          "supranuclear palsy, progressive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia."
      },
      "child_count": 16,
      "reference_id": "MONDO:0019037"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18949,
      "label": "progressive supranuclear palsy"
    }
  ]
}