{
  "id": 23192,
  "label": "amyopathic dermatomyositis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0043317",
  "properties": {
    "xrefs": [
      "GARD:0009907",
      "MEDGEN:96065",
      "MESH:C538250",
      "NANDO:1200275",
      "Orphanet:645617",
      "SCTID:238935002",
      "UMLS:C0406645",
      "icd11.foundation:727262285"
    ],
    "synonyms": [
      "amyopathic dermatomyositis",
      "dermatomyositis sine myositis",
      "ADM"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "A form of dermatomyositis characterized by the presence of typical skin finding swithout muscle weakness. Some of the skin changes that suggest dermatomyositis include a pink rash on the face, neck, forearms and upper chest; Gottron's papules and heliotrope eyelids. Pruritis and photosensitivity are common, as is scalp inflammation and thinning of the hair.While patients with amyopathic dermatomyositis should not have clinically evident muscle weakness, minor muscle abnormalities may be included.Fatigue is reported in at least 50% of patients. Some cases have beenassociated with internal malignancy and/or interstitial lung disease. Treatment may include sun avoidance, ample use of sunscreen, topical corticosteroids, antimalarial agents, methotrexate, mycophenolate mofetil, or intravenous (IV) immunoglobulin."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 26518,
      "label": "clinically amyopathic dermatomyositis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027229"
        ],
        "synonyms": [
          "CADM",
          "anti-MDA5 dermatomyositis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A dermatomyositis with cutaneous features but no skeletal muscle weakness."
      },
      "child_count": 2,
      "reference_id": "MONDO:1010096"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 26518,
      "label": "clinically amyopathic dermatomyositis"
    }
  ]
}