{
  "id": 4419,
  "label": "retinal vascular disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002311",
  "properties": {
    "xrefs": [
      "DOID:2462",
      "ICD9:362.13",
      "MEDGEN:57824",
      "NCIT:C35170",
      "SCTID:57534004",
      "UMLS:C0154833"
    ],
    "synonyms": [
      "retinal vascular disorder"
    ],
    "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": "Retinal damage resulting from diminished blood flow/oxygenation due to abnormalities of the retinal vessels. Causes include hypertension, diabetes, thrombosis, embolism, and hemorrhage."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 12,
  "parents": [
    {
      "id": 6979,
      "label": "retinal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799,
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5679",
          "EFO:0003839",
          "HGNC:8002",
          "ICD9:362.89",
          "ICD9:362.9",
          "MEDGEN:11209",
          "MESH:D012164",
          "NCIT:C26875",
          "NCIT:C62601",
          "SCTID:29555009",
          "UMLS:C0035309"
        ],
        "synonyms": [
          "eye disease of retina",
          "retina eye disease",
          "retinopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any disease or disorder of the retina."
      },
      "child_count": 64,
      "reference_id": "MONDO:0005283"
    },
    {
      "id": 7202,
      "label": "ocular vascular disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019,
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005753",
          "MEDGEN:182689",
          "NCIT:C35664",
          "UMLS:C0948522"
        ],
        "synonyms": [
          "disease of vasculature of eye",
          "disease or disorder of vasculature of eye",
          "disorder of vasculature of eye",
          "ocular vascular disorder",
          "vasculature of eye disease",
          "vasculature of eye disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A disorder that is caused by pathologic changes in the ocular vasculature."
      },
      "child_count": 6,
      "reference_id": "MONDO:0005552"
    },
    {
      "id": 23165,
      "label": "neurovascular disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799,
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:857738",
          "NCIT:C117007",
          "UMLS:C3898144"
        ],
        "synonyms": [
          "disease of nervous system vasculature",
          "nervous system disorder of vasculature",
          "neurovascular disorder",
          "vasculature nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disorder of the nervous system related to a vascular etiology."
      },
      "child_count": 58,
      "reference_id": "MONDO:0043218"
    }
  ],
  "children": [
    {
      "id": 3494,
      "label": "retinal microaneurysm",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11295",
          "ICD9:362.14",
          "MEDGEN:472899",
          "SCTID:34037000",
          "UMLS:C0154834"
        ],
        "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:0001257"
    },
    {
      "id": 4229,
      "label": "retinal vascular occlusion",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4419,
        20082
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1729",
          "ICD10CM:H34",
          "ICD9:362.3",
          "ICD9:362.30",
          "MEDGEN:19762",
          "NCIT:C34980",
          "SCTID:73757007",
          "UMLS:C0035326"
        ],
        "synonyms": [
          "retinal vascular occlusion",
          "retinal vascular occlusion, unspecified"
        ],
        "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": "An occlusion of the retinal vasculature."
      },
      "child_count": 4,
      "reference_id": "MONDO:0002089"
    },
    {
      "id": 5279,
      "label": "retinal hemangioblastoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4419,
        17196,
        20657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5240",
          "GARD:0023461",
          "MEDGEN:152677",
          "NCIT:C39783",
          "UMLS:C0730303"
        ],
        "synonyms": [
          "hemangioblastoma of vasculature of retina",
          "retinal capillary hemangioblastoma",
          "retinal hemangioblastoma",
          "vasculature of retina hemangioblastoma"
        ],
        "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 hemangioblastoma that arises from the retina. It is typically a sign of von Hippel-Lindau disease. It may also be seen as an isolated entity without systemic involvement."
      },
      "child_count": 3,
      "reference_id": "MONDO:0003343"
    },
    {
      "id": 6162,
      "label": "retinal telangiectasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:7736",
          "HP:0007763",
          "ICD9:362.15",
          "MEDGEN:57598",
          "SCTID:84884003",
          "UMLS:C0154835"
        ],
        "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": 1,
      "reference_id": "MONDO:0004348"
    },
    {
      "id": 6966,
      "label": "diabetic retinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4419,
        6795
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8947",
          "EFO:0003770",
          "ICD9:362.0",
          "MEDGEN:3786",
          "MESH:D003930",
          "NCIT:C34538",
          "SCTID:4855003",
          "UMLS:C0011884",
          "icd11.foundation:1006882070"
        ],
        "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 chronic, pathological complication associated with diabetes mellitus, where retinal damages are incurred due to microaneurysms in the vasculature of the retina, progressively leading to abnormal blood vessel growth, and swelling and leaking of fluid from blood vessels, resulting in vision loss or blindness."
      },
      "child_count": 6,
      "reference_id": "MONDO:0005266"
    },
    {
      "id": 8379,
      "label": "retinal vasculitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4419,
        4749,
        18813
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11563",
          "EFO:1001156",
          "GARD:0024505",
          "ICD10CM:H35.06",
          "ICD9:362.18",
          "MEDGEN:57503",
          "MESH:D031300",
          "MedDRA:10038905",
          "SCTID:77628002",
          "UMLS:C0152026",
          "icd11.foundation:1863208483"
        ],
        "synonyms": [
          "retinal vasculitis"
        ],
        "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": "Inflammation of the retinal vasculature with various causes including infectious disease; lupus erythematosus, systemic; multiple sclerosis; behcet syndrome; and chorioretinitis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006950"
    },
    {
      "id": 9923,
      "label": "retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4419,
        19000,
        24651,
        25666
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111567",
          "GARD:0001217",
          "MEDGEN:348124",
          "MESH:C566007",
          "NORD:1910",
          "OMIM:192315",
          "Orphanet:247691",
          "SCTID:720854004",
          "SCTID:721141004",
          "UMLS:C1860518",
          "icd11.foundation:554838792"
        ],
        "synonyms": [
          "RVCL",
          "RVCL-S",
          "hereditary vascular retinopathy",
          "retinal vasculopathy and cerebral leukoencephalopathy",
          "vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestations",
          "ADRVCL",
          "CRV",
          "HVR",
          "autosomal dominant retinal vasculopathy with cerebral leukodystrophy",
          "cerebroretinal vasculopathy",
          "cerebroretinal vasculopathy, hereditary",
          "grand Kaine fulling syndrome",
          "grand-Kaine-fulling syndrome",
          "retinal vasculopathy with cerebral leukodystrophy",
          "retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena",
          "vasculopathy, retinal, with cerebral leukodystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008641"
    },
    {
      "id": 14665,
      "label": "familial retinal arterial macroaneurysm",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4419,
        24270,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012779",
          "MEDGEN:481835",
          "OMIM:614224",
          "Orphanet:284247",
          "SCTID:764452004",
          "UMLS:C3280205",
          "icd11.foundation:800928909"
        ],
        "synonyms": [
          "FRAM",
          "Fram",
          "retinal arterial macroaneurysm and supravalvular pulmonic stenosis",
          "RAMSVPS",
          "retinal arterial macroaneurysm with supravalvular pulmonic stenosis"
        ],
        "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:0013640"
    },
    {
      "id": 18293,
      "label": "vasoproliferative tumor of retina",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3034,
        4419,
        20575,
        21330
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021533",
          "MEDGEN:1652844",
          "Orphanet:353356",
          "UMLS:C4749792"
        ],
        "synonyms": [
          "VPTR",
          "retinal vasoproliferative tumor",
          "retinal vasoproliferative tumour",
          "vasoproliferative tumor of ocular fundus",
          "vasoproliferative tumor of the ocular fundus",
          "vasoproliferative tumour of ocular fundus",
          "vasoproliferative tumour of the ocular fundus",
          "vasoproliferative tumor of the retina",
          "vasoproliferative tumour of the retina"
        ],
        "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": "Vasoproliferative tumor of the retina is a rare, benign, retinal vascular disease characterized by solitary or multiple, unilateral or bilateral, intra-retinal tumor(s), usually located in the peripheral infero-temporal quadrant, and often associated with sub- and intraretinal exudates, epiretinal membranes, exudative retinal detachment and cystoid macular edema, as well as, occasionally, retinal and vitreous hemorrhage. Patients may present with visual loss, floaters, and/or photopsia. Association with various conditions, such as retinitis pigmentosa, congenital retinal toxoplasmosis, retinopathy of prematurity, or coloboma, has been reported."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018148"
    },
    {
      "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"
    },
    {
      "id": 23068,
      "label": "arteriosclerotic retinopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4391,
        4419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:440.8",
          "MEDGEN:573178",
          "SCTID:95691008",
          "UMLS:C0339478"
        ],
        "synonyms": [
          "arteriosclerosis disorder of retina",
          "arteriosclerotic retinopathy",
          "retina arteriosclerosis disorder",
          "arteriosclerosis, retina",
          "retinal arteriosclerosis",
          "retinopathy, arteriosclerotic"
        ],
        "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 arteriosclerosis disorder that involves the retina."
      },
      "child_count": 0,
      "reference_id": "MONDO:0042495"
    },
    {
      "id": 26056,
      "label": "perifoveal exudative vascular anomalous complex",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027187",
          "MEDGEN:1863553",
          "Orphanet:674930",
          "UMLS:C5925081"
        ],
        "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:0971124"
    }
  ],
  "roots": [
    {
      "id": 6979,
      "label": "retinal disorder"
    },
    {
      "id": 7202,
      "label": "ocular vascular disorder"
    },
    {
      "id": 23165,
      "label": "neurovascular disorder"
    }
  ]
}