{
  "id": 15620,
  "label": "Brown syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014624",
  "properties": {
    "xrefs": [
      "DOID:10235",
      "ICD10CM:H50.61",
      "ICD9:378.61",
      "MEDGEN:102332",
      "OMIM:616407",
      "SCTID:35929003",
      "UMLS:C0155339"
    ],
    "synonyms": [
      "BRWNS",
      "Brown syndrome",
      "Brown tendon sheath syndrome",
      "Brown's (tendon) sheath syndrome",
      "Brown's sheath syndrome",
      "Brown's tendon sheath syndrome",
      "superior oblique tendon sheath syndrome",
      "tendon sheath adherence, Superior oblique"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Brown syndrome is a rare eye disorder characterized by defects in eye movements caused by abnormalities of the superior oblique tendon sheath of the superior oblique muscle."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6524,
      "label": "mechanical strabismus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9306",
          "ICD10CM:H50.6",
          "ICD9:378.6",
          "ICD9:378.60",
          "MEDGEN:101828",
          "SCTID:5371001",
          "UMLS:C0152223",
          "icd11.foundation:230827382"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0004753"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6524,
      "label": "mechanical strabismus"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}