{
  "id": 18949,
  "label": "progressive supranuclear palsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019037",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 7073,
      "label": "movement disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:480",
          "EFO:0004280",
          "ICD9:333.90",
          "ICD9:333.99",
          "MEDGEN:10113",
          "MESH:D009069",
          "NCIT:C116757",
          "SCTID:60342002",
          "UMLS:C0026650"
        ],
        "synonyms": [
          "movement disease",
          "movement disorder",
          "movement disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement."
      },
      "child_count": 54,
      "reference_id": "MONDO:0005395"
    },
    {
      "id": 19772,
      "label": "supranuclear oculomotor palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3541
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019546",
          "MEDGEN:1842980",
          "Orphanet:98687",
          "UMLS:C5681698"
        ],
        "synonyms": [
          "supranuclear eye movement disorder",
          "conjugate gaze palsy",
          "gaze palsy",
          "supranuclear disorder of eye movement",
          "supranuclear ocular palsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Oculomotor palsy that arises from lesions in the supranuclear pathways controlling extraocular movement."
      },
      "child_count": 1,
      "reference_id": "MONDO:0020257"
    },
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020280",
          "MEDGEN:1825988",
          "MESH:D020271",
          "NCIT:C97073",
          "Orphanet:183500",
          "UMLS:C5680568"
        ],
        "synonyms": [
          "genetic neurodegenerative disease",
          "hereditary neurodegenerative disease",
          "hereditary neurodegenerative disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An inherited disorder characterized by progressive degeneration and atrophy of the nervous system."
      },
      "child_count": 164,
      "reference_id": "MONDO:0024237"
    }
  ],
  "children": [
    {
      "id": 12123,
      "label": "supranuclear palsy, progressive, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18949
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010997"
    },
    {
      "id": 13337,
      "label": "supranuclear palsy, progressive, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18949
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018344",
          "MEDGEN:324446",
          "MESH:C563717",
          "OMIM:609454",
          "UMLS:C1836148"
        ],
        "synonyms": [
          "PSNP2",
          "supranuclear palsy, progressive, 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012278"
    },
    {
      "id": 13623,
      "label": "supranuclear palsy, progressive, 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18949
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018345",
          "MEDGEN:370922",
          "MESH:C567050",
          "OMIM:610898",
          "UMLS:C1970476"
        ],
        "synonyms": [
          "PSNP3",
          "supranuclear palsy, progressive, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012576"
    },
    {
      "id": 19943,
      "label": "atypical progressive supranuclear palsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18949
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004507",
          "MEDGEN:1779597",
          "Orphanet:99750",
          "UMLS:C5548371"
        ],
        "synonyms": [
          "atypical PSP syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Atypical progressive supranuclear palsy (atypical PSP) is a group of clinical syndromes associated with underlying PSP-tau pathology, that do not conform to the classic presentation of PSP (Richardson syndrome), a rare late-onset neurodegenerative disease. The group comprises PSP-Parkinsonism (PSP-P), PSP-Pure akinesia with gait freezing (PSP-PAGF), PSP-corticobasal syndrome (PSP-CBS) and PSP-progressive non fluent aphasia (PSP-PNFA)."
      },
      "child_count": 4,
      "reference_id": "MONDO:0020488"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 7073,
      "label": "movement disorder"
    },
    {
      "id": 19772,
      "label": "supranuclear oculomotor palsy"
    },
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder"
    }
  ]
}