{
  "id": 9782,
  "label": "stiff-person syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008491",
  "properties": {
    "xrefs": [
      "DOID:13366",
      "EFO:0007498",
      "GARD:0005023",
      "ICD10CM:G25.82",
      "ICD9:333.91",
      "MEDGEN:39017",
      "MESH:D016750",
      "MedDRA:10042044",
      "NCIT:C85170",
      "NORD:1740",
      "OMIM:184850",
      "Orphanet:3198",
      "SCTID:5217008",
      "UMLS:C0085292"
    ],
    "synonyms": [
      "Moersch-Woltman syndrome",
      "Stiff Person Syndrome",
      "Stiff Person syndrome",
      "Stiff-man syndrome",
      "stiff-person syndrome",
      "Morsch Woltman syndrome",
      "SMS",
      "SPS",
      "STIFF-PERSON syndrome",
      "Stiff person syndrome and related disorders",
      "Stiff-Man syndrome",
      "Stiff-trunk syndrome",
      "progressive encephalomyelitis with rigidity"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Stiff-man syndrome (SMS) is a rare neurological disorder comprising fluctuating trunk and limb stiffness, painful muscle spasms, task-specific phobia, an exaggerated startle response, and ankylosing deformities such as fixed lumbar hyperlordosis."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "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": 6799,
      "label": "nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:863",
          "EFO:0000618",
          "ICD10CM:G00-G99",
          "ICD9:349.89",
          "ICD9:349.9",
          "MEDGEN:14336",
          "MESH:D009422",
          "NCIT:C26835",
          "SCTID:118940003",
          "UMLS:C0027765",
          "Wikipedia:Nervous_system_disease"
        ],
        "synonyms": [
          "disease of nervous system",
          "disease or disorder of nervous system",
          "disorder of nervous system",
          "nervous system disease",
          "nervous system disease or disorder",
          "nervous system disorder",
          "neurologic disease",
          "neurologic disorder",
          "neurological disease",
          "neurological disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the brain, spinal cord, or peripheral nerves."
      },
      "child_count": 72,
      "reference_id": "MONDO:0005071"
    }
  ],
  "children": [
    {
      "id": 18585,
      "label": "progressive encephalomyelitis with rigidity and myoclonus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9782
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0013110",
          "MEDGEN:349287",
          "Orphanet:438266",
          "UMLS:C1861457"
        ],
        "synonyms": [
          "PERM",
          "progressive encephalomyelitis with rigidity"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018581"
    },
    {
      "id": 18623,
      "label": "classic stiff person syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9782
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017754",
          "MEDGEN:1842410",
          "Orphanet:443192",
          "UMLS:C5680058"
        ],
        "synonyms": [
          "classic SPS"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018625"
    },
    {
      "id": 18626,
      "label": "focal stiff limb syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9782
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017756",
          "MEDGEN:1672496",
          "Orphanet:443804",
          "UMLS:C4324606"
        ],
        "synonyms": [
          "Stiff leg syndrome",
          "focal stiff-person syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018629"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 6799,
      "label": "nervous system disorder"
    }
  ]
}