{
  "id": 6517,
  "label": "myopathy of extraocular muscle",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004746",
  "properties": {
    "xrefs": [
      "DOID:929",
      "GARD:0024100",
      "ICD10CM:H05.82",
      "ICD9:376.82",
      "MEDGEN:509895",
      "SCTID:57130002",
      "UMLS:C0155286"
    ],
    "synonyms": [
      "extra-ocular muscle myopathy",
      "myopathy of extra-ocular muscle",
      "myopathy of extraocular muscles"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A myopathy that involves the extra-ocular muscle."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 2924,
      "label": "eye adnexa disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4171
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050815",
          "EFO:0009546",
          "ICD10WHO:H00-H06",
          "MEDGEN:713201",
          "SCTID:118941004",
          "UMLS:C1290855"
        ],
        "synonyms": [
          "disease of ocular adnexa",
          "disease or disorder of ocular adnexa",
          "disorder of ocular adnexa",
          "ocular adnexa disease",
          "ocular adnexa disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          }
        ],
        "definition": "A disease involving the ocular adnexa."
      },
      "child_count": 6,
      "reference_id": "MONDO:0000462"
    },
    {
      "id": 7023,
      "label": "myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19743
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:423",
          "EFO:0004145",
          "ICD9:359.8",
          "ICD9:359.9",
          "ICD9:728.3",
          "MEDGEN:10135",
          "NCIT:C101216",
          "SCTID:129565002",
          "UMLS:C0026848",
          "icd11.foundation:1870184184"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease of the muscle in which the muscle fibers do not function properly. This results in muscular weakness."
      },
      "child_count": 32,
      "reference_id": "MONDO:0005336"
    },
    {
      "id": 21415,
      "label": "disorder of visual system",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "SCTID:128127008"
        ],
        "synonyms": [
          "disease of visual system",
          "disease or disorder of visual system",
          "disorder of visual system",
          "visual system disease",
          "visual system disease or disorder",
          "visual system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A disease that involves the visual system."
      },
      "child_count": 30,
      "reference_id": "MONDO:0024458"
    }
  ],
  "children": [
    {
      "id": 8980,
      "label": "congenital fibrosis of extraocular muscles",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3785,
        6517,
        16732
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080143",
          "GARD:0012590",
          "ICD9:728.2",
          "MEDGEN:724506",
          "MESH:C580012",
          "NORD:997",
          "OMIMPS:135700",
          "Orphanet:45358",
          "SCTID:400946004",
          "UMLS:C1302995",
          "icd11.foundation:887449084"
        ],
        "synonyms": [
          "Congenital Fibrosis of the Extraocular Muscles",
          "FEOM",
          "congenital fibrosis of the extraocular muscles",
          "fibrosis of extraocular muscles, congenital",
          "fibrosis of extraocular muscles, congenital, type 1",
          "Tukel syndrome",
          "CFEOM1",
          "Feom1 locus",
          "blepharoptosis with absent eye movements",
          "fibrosis of extraocular muscles, congenital, 1",
          "fibrosis of extraocular muscles, congenital, 3B",
          "ophthalmoplegia, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 24,
      "reference_id": "MONDO:0007614"
    },
    {
      "id": 9432,
      "label": "oculopharyngeal muscular dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6517,
        16732
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11719",
          "GARD:0007245",
          "MEDGEN:75730",
          "MESH:D039141",
          "MedDRA:10052181",
          "NANDO:1200493",
          "NORD:1523",
          "OMIMPS:164300",
          "Orphanet:270",
          "SCTID:77097004",
          "UMLS:C0270952",
          "icd11.foundation:1354386293"
        ],
        "synonyms": [
          "OPMD",
          "oculopharyngeal muscular dystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Oculopharyngeal muscular dystrophy (OPMD) is an adult-onset progressive myopathy characterized by progressive eyelid ptosis, dysphagia, dysarthria and proximal limb weakness."
      },
      "child_count": 4,
      "reference_id": "MONDO:0008116"
    },
    {
      "id": 24275,
      "label": "orbital myositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6517,
        20400
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026276",
          "ICD10CM:H05.12",
          "ICD9:376.12",
          "MEDGEN:389999",
          "NCIT:C117296",
          "SCTID:80698001",
          "UMLS:C2350476"
        ],
        "synonyms": [
          "ocular myositis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A rare form of myositis that affects only the orbital muscles."
      },
      "child_count": 0,
      "reference_id": "MONDO:0100550"
    }
  ],
  "roots": [
    {
      "id": 2924,
      "label": "eye adnexa disorder"
    },
    {
      "id": 7023,
      "label": "myopathy"
    },
    {
      "id": 21415,
      "label": "disorder of visual system"
    }
  ]
}