{
  "id": 9377,
  "label": "juvenile dermatomyositis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008054",
  "properties": {
    "xrefs": [
      "DOID:14203",
      "EFO:0000557",
      "GARD:0006805",
      "ICD10CM:M33.0",
      "MEDGEN:120486",
      "MESH:C000598745",
      "MedDRA:10008521",
      "NANDO:2200418",
      "NCIT:C27576",
      "Orphanet:93672",
      "SCTID:1212005",
      "UMLS:C0263666",
      "icd11.foundation:1428089375"
    ],
    "synonyms": [
      "childhood dermatomyositis",
      "inflammation of myoseptum",
      "juvenile DM",
      "juvenile dermatomyositis",
      "myoseptum inflammation",
      "myoseptumitis",
      "JDM",
      "JPM",
      "childhood type dermatomyositis",
      "juvenile myositis",
      "myopathy, familial idiopathic inflammatory",
      "myositis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "Juvenile dermatomyositis (JDM) is the early-onset form of dermatomyositis (DM), a systemic, autoimmune inflammatory muscle disorder, characterized by proximal muscle weakness, evocative skin lesion, and systemic manifestations."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16899,
      "label": "dermatomyositis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4496,
        7203,
        19007
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10223",
          "EFO:0000398",
          "GARD:0006263",
          "ICD10CM:M33",
          "ICD9:710.3",
          "MEDGEN:8331",
          "MESH:D003882",
          "MedDRA:10012503",
          "NANDO:1200274",
          "NCIT:C26744",
          "NORD:1048",
          "Orphanet:221",
          "SCTID:396230008",
          "UMLS:C0011633",
          "icd11.foundation:739030149"
        ],
        "synonyms": [
          "DM",
          "dermatomyositis",
          "dermatopolymyositis",
          "adult dermatomyositis",
          "Amyopathic dermatomyositis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness."
      },
      "child_count": 33,
      "reference_id": "MONDO:0016367"
    },
    {
      "id": 18185,
      "label": "juvenile idiopathic inflammatory myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19745
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021496",
          "MEDGEN:1842624",
          "Orphanet:329888",
          "UMLS:C5679857"
        ],
        "synonyms": [
          "JIIM"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0018010"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16899,
      "label": "dermatomyositis"
    },
    {
      "id": 18185,
      "label": "juvenile idiopathic inflammatory myopathy"
    }
  ]
}