{
  "id": 29271,
  "label": "FZD4-related exudative vitreoretinopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:1040041",
  "properties": {
    "xrefs": [
      "GARD:0027243"
    ],
    "synonyms": [
      "FZD4-related exudative vitreoretinopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Any exudative vitreoretinopathy caused by a variant in the FZD4 gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19329,
      "label": "exudative vitreoretinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4419,
        19768
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050535",
          "GARD:0001613",
          "ICD9:362.10",
          "MEDGEN:573220",
          "MESH:C580083",
          "OMIMPS:133780",
          "Orphanet:891",
          "SCTID:232063007",
          "UMLS:C0339539"
        ],
        "synonyms": [
          "Criswick-Schepens syndrome",
          "FEVR",
          "familial exudative vitreoretinopathy",
          "exudative vitreoretinopathy, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Familial exudative vitreoretinopathy (FEVR) is a rare hereditary vitreoretinal disorder characterized by abnormal or incomplete vascularization of the peripheral retina leading to variable clinical manifestations ranging from no effects to minor anomalies, or even retinal detachment with blindness."
      },
      "child_count": 18,
      "reference_id": "MONDO:0019516"
    }
  ],
  "children": [
    {
      "id": 8381,
      "label": "retinopathy of prematurity",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        29271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13025",
          "EFO:1001158",
          "GARD:0005695",
          "ICD10CM:H35.1",
          "ICD10CM:H35.17",
          "ICD9:362.20",
          "ICD9:362.21",
          "MEDGEN:48438",
          "MESH:D012178",
          "MedDRA:10038933",
          "NCIT:C34982",
          "NORD:1663",
          "Orphanet:90050",
          "SCTID:415297005",
          "UMLS:C0035344",
          "icd11.foundation:947283385"
        ],
        "synonyms": [
          "ROP",
          "Terry syndrome",
          "retrolental fibroplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A bilateral retinopathy characterized by neovascularization, scarring, retinal detachment, and eventually blindness. It may be mild or severe. It occurs in babies born prematurely. Causes include oxygen toxicity and hypoxia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006952"
    },
    {
      "id": 8961,
      "label": "exudative vitreoretinopathy 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        29271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111412",
          "GARD:0015068",
          "MEDGEN:343561",
          "MESH:C536382",
          "NCIT:C175048",
          "OMIM:133780",
          "UMLS:C1851402"
        ],
        "synonyms": [
          "exudative vitreoretinopathy 1",
          "exudative vitreoretinopathy type 1",
          "Criswick-Schepens syndrome",
          "EVR1",
          "FEVR, autosomal dominant",
          "exudative vitreoretinopathy, familial, autosomal dominant",
          "retinopathy of prematurity"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007589"
    }
  ],
  "roots": [
    {
      "id": 19329,
      "label": "exudative vitreoretinopathy"
    }
  ]
}