{
  "id": 19182,
  "label": "antisynthetase syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019344",
  "properties": {
    "xrefs": [
      "DOID:0080744",
      "EFO:1001982",
      "GARD:0000735",
      "ICD9:279.49",
      "MEDGEN:1866768",
      "MESH:C537778",
      "MedDRA:10068801",
      "NORD:1926",
      "Orphanet:81",
      "SCTID:445187004",
      "UMLS:C5959873",
      "icd11.foundation:1572057936"
    ],
    "synonyms": [
      "AS syndrome",
      "anti-Jo1 syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Antisynthetase (AS) syndrome is a clinically heterogeneous form of idiopathic inflammatory myopathy characterized by myositis, arthralgia, Raynaud phenomenon, mechanic hands, interstitial lung disease (ILD), and serum autoantibodies to aminoacyl transfer RNA synthetases (anti-ARS)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19745,
      "label": "acquired idiopathic inflammatory myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16731,
        24391,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009128",
          "ICD9:359.79",
          "Orphanet:98482",
          "icd11.foundation:464294586"
        ],
        "synonyms": [
          "IIm",
          "IMM",
          "idiopathic inflammatory myopathies",
          "idiopathic inflammatory myositis",
          "idiopathic inflammatory myopathy, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An umbrella term for diseases which have chronic muscle inflammation and weakness of unknown etiology. The types of idiopathic inflammatory myopathy are further defined by either clinicopathologic criteria or by the presence of certain autoantibodies."
      },
      "child_count": 27,
      "reference_id": "MONDO:0020122"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19745,
      "label": "acquired idiopathic inflammatory myopathy"
    }
  ]
}