{
  "id": 13344,
  "label": "Stickler syndrome, type I, nonsyndromic ocular",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012287",
  "properties": {
    "xrefs": [
      "GARD:0015461",
      "MEDGEN:322820",
      "MESH:C563709",
      "OMIM:609508",
      "UMLS:C1836080"
    ],
    "synonyms": [
      "Stickler syndrome, type i, nonsyndromic ocular",
      "Stickler syndrome, atypical",
      "Stickler syndrome, type I, predominantly ocular",
      "rhegmatogenous retinal detachment, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8567,
      "label": "Stickler syndrome type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19190,
        20997,
        24324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080676",
          "GARD:0005018",
          "MEDGEN:810955",
          "MESH:C537492",
          "NANDO:2201354",
          "NCIT:C168733",
          "OMIM:108300",
          "Orphanet:90653",
          "UMLS:C2020284",
          "icd11.foundation:203625278"
        ],
        "synonyms": [
          "Stickler syndrome type 1",
          "STL1",
          "Stickler syndrome, membranous vitreous type",
          "Stickler syndrome, type 1",
          "Stickler syndrome, type I",
          "Stickler syndrome, vitreous type 1",
          "arthroophthalmopathy, hereditary progressive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0007160"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8567,
      "label": "Stickler syndrome type 1"
    }
  ]
}