{
  "id": 16899,
  "label": "dermatomyositis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016367",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 11,
  "parents": [
    {
      "id": 4496,
      "label": "dermatitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2723",
          "ICD9:692.9",
          "MEDGEN:849741",
          "MESH:D003872",
          "NCIT:C2983",
          "SCTID:43116000",
          "UMLS:C3875321"
        ],
        "synonyms": [
          "inflammation of skin",
          "inflammation of the skin",
          "inflammation of zone of skin",
          "inflammatory skin disease",
          "skin inflammation",
          "zone of skin inflammation"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An inflammatory process affecting the skin. Signs include red rash, itching, and blister formation. Representative examples are contact dermatitis, atopic dermatitis, and seborrheic dermatitis."
      },
      "child_count": 66,
      "reference_id": "MONDO:0002406"
    },
    {
      "id": 7203,
      "label": "rheumatic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1575",
          "EFO:0005755",
          "ICD9:729.0",
          "MEDGEN:3157",
          "MESH:D012216",
          "NANDO:2100151",
          "NANDO:2100152",
          "NCIT:C27204",
          "SCTID:396332003",
          "UMLS:C0009326",
          "Wikipedia:Rheumatism"
        ],
        "synonyms": [
          "rheumatic disease",
          "rheumatologic disorder",
          "collagen disease",
          "collagen vascular disease",
          "connective tissue disease",
          "disease, rheumatic",
          "diseases, rheumatic",
          "enthesopathies",
          "enthesopathy",
          "inflammatory rheumatism",
          "musculoskeletal pain disorder",
          "rheumatism"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Inflammatory and degenerative diseases of connective tissue structures, such as arthritis."
      },
      "child_count": 30,
      "reference_id": "MONDO:0005554"
    },
    {
      "id": 19007,
      "label": "polymyositis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19745
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080745",
          "EFO:0003063",
          "GARD:0007425",
          "ICD10CM:M33.2",
          "ICD9:710.4",
          "MEDGEN:39086",
          "MESH:D017285",
          "MedDRA:10036102",
          "NANDO:1200276",
          "NCIT:C26925",
          "Orphanet:732",
          "SCTID:31384009",
          "UMLS:C0085655",
          "Wikipedia:Polymyositis",
          "icd11.foundation:1157134196"
        ],
        "synonyms": [
          "PM",
          "polymyositis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019127"
    }
  ],
  "children": [
    {
      "id": 4080,
      "label": "adult dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14202",
          "GARD:0023038",
          "MEDGEN:66356",
          "NCIT:C27313",
          "SCTID:402425006",
          "UMLS:C0221056",
          "icd11.foundation:544509908"
        ],
        "synonyms": [
          "dermatomyositis of adults"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Dermatomyositis in an adult."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001907"
    },
    {
      "id": 9377,
      "label": "juvenile dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899,
        18185
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008054"
    },
    {
      "id": 18442,
      "label": "neonatal dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3005,
        16899,
        18439
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021646",
          "MEDGEN:1649267",
          "Orphanet:398117",
          "UMLS:C4751516"
        ],
        "synonyms": [
          "neonatal DM"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018359"
    },
    {
      "id": 25681,
      "label": "classical dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026836",
          "MEDGEN:1843411",
          "Orphanet:645613",
          "UMLS:C5816707"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957456"
    },
    {
      "id": 25682,
      "label": "adermatopathic dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026837",
          "MEDGEN:1843427",
          "Orphanet:645626",
          "UMLS:C5816708"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957458"
    },
    {
      "id": 26486,
      "label": "anti-MDA5 dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027223"
        ],
        "synonyms": [
          "MDA-5 DM",
          "MDA5+ DM",
          "anti-melanoma differentiation-associated gene 5 dermatomyositis",
          "clinically 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": "A dermatomyositis characterized by the presence of anti-MDA5 autoantibodies. It is often associated with dermatomyositis rashes, amyopathic or hypomyopathic muscle involvement and interstitial lung disease, frequently as a rapid progressive course and high mortality."
      },
      "child_count": 0,
      "reference_id": "MONDO:1010064"
    },
    {
      "id": 26487,
      "label": "anti-Mi2 dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027224"
        ],
        "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 characterized by the presence of anti-Mi2 autoantibodies."
      },
      "child_count": 0,
      "reference_id": "MONDO:1010065"
    },
    {
      "id": 26506,
      "label": "anti-NXP2 dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027225"
        ],
        "synonyms": [
          "anti-nuclear matrix protein 2 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 characterized by the presence of anti-NXP2 autoantibodies."
      },
      "child_count": 0,
      "reference_id": "MONDO:1010084"
    },
    {
      "id": 26509,
      "label": "anti-TIF1 dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027226"
        ],
        "synonyms": [
          "anti-transcription intermediary factor 1 complex 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 characterized by the presence of anti-TIF1 autoantibodies."
      },
      "child_count": 0,
      "reference_id": "MONDO:1010087"
    },
    {
      "id": 26510,
      "label": "anti-SAE dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16899
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027227"
        ],
        "synonyms": [
          "anti-small ubiquitin-like modifier activating enzyme 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 characterized by the presence of anti-SAE autoantibodies."
      },
      "child_count": 0,
      "reference_id": "MONDO:1010088"
    },
    {
      "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"
    }
  ],
  "roots": [
    {
      "id": 4496,
      "label": "dermatitis"
    },
    {
      "id": 7203,
      "label": "rheumatic disorder"
    },
    {
      "id": 19007,
      "label": "polymyositis"
    }
  ]
}