{
  "id": 4072,
  "label": "optic choroid disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001898",
  "properties": {
    "xrefs": [
      "DOID:1417",
      "ICD9:363.8",
      "ICD9:363.9",
      "MEDGEN:892839",
      "MESH:D015862",
      "NCIT:C34468",
      "SCTID:128468007",
      "UMLS:C4025836"
    ],
    "synonyms": [
      "choroid disorder",
      "disease of optic choroid",
      "disease or disorder of optic choroid",
      "disorder of optic choroid",
      "optic choroid disease",
      "optic choroid disease or disorder",
      "choroid disease"
    ],
    "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 disease involving the optic choroid."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 7,
  "parents": [
    {
      "id": 4712,
      "label": "uveal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3480",
          "MEDGEN:21804",
          "MESH:D014603",
          "NCIT:C26908",
          "SCTID:95678007",
          "UMLS:C0042161"
        ],
        "synonyms": [
          "disease of uvea",
          "disease or disorder of uvea",
          "disorder of uvea",
          "uvea disease",
          "uvea disease or disorder",
          "uveal disease",
          "uveal disorder",
          "uveal tract disease",
          "disorder of uveal tract",
          "uveal diseases"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the uvea. Representative examples include uveitis, chorioretinitis, and uveal melanoma."
      },
      "child_count": 4,
      "reference_id": "MONDO:0002661"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 3514,
      "label": "choroiditis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4072,
        8351,
        18813
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11406",
          "GARD:0004457",
          "HP:0012123",
          "MEDGEN:40282",
          "MESH:D002833",
          "MedDRA:10036370",
          "NCIT:C35111",
          "NORD:1601",
          "Orphanet:280892",
          "SCTID:16553002",
          "UMLS:C0008526",
          "icd11.foundation:1884626736"
        ],
        "synonyms": [
          "Choroiditides",
          "choroiditis",
          "Posterior Uveitis",
          "posterior uveitis",
          "posterior uveitis (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An inflammatory process that affects the choroid."
      },
      "child_count": 12,
      "reference_id": "MONDO:0001280"
    },
    {
      "id": 3860,
      "label": "retinal dystrophies primarily involving Bruch's membrane",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4072,
        19000,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13227",
          "GARD:0022986",
          "ICD9:362.77",
          "MEDGEN:1720702",
          "UMLS:C0154866"
        ],
        "synonyms": [
          "Bruch's membrane inherited retinal dystrophy",
          "inherited retinal dystrophy of Bruch's membrane"
        ],
        "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 retinal dystrophy with etiology arising from Bruch's membrane, the site of drusen generation."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001666"
    },
    {
      "id": 6640,
      "label": "choroidal sclerosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4072,
        6639,
        7208,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:980",
          "ICD9:363.4",
          "ICD9:363.40",
          "MEDGEN:137998",
          "MESH:C535358",
          "SCTID:406446000",
          "UMLS:C0344297"
        ],
        "synonyms": [
          "choroidal degenerations",
          "neurodegenerative disease of optic choroid",
          "optic choroid neurodegenerative disease"
        ],
        "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 neurodegenerative disease that involves the optic choroid."
      },
      "child_count": 16,
      "reference_id": "MONDO:0004885"
    },
    {
      "id": 10240,
      "label": "central areolar choroidal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4072,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010049",
          "ICD10CM:H31.22",
          "ICD9:363.54",
          "MEDGEN:283932",
          "NANDO:1200939",
          "OMIMPS:215500",
          "Orphanet:75377",
          "SCTID:231996009",
          "SCTID:312918002",
          "UMLS:C1536451",
          "icd11.foundation:2018537024"
        ],
        "synonyms": [
          "CACD",
          "areolar atrophy of the macula",
          "central areolar choroidal sclerosis",
          "choroidal dystrophy",
          "CACD1",
          "choroidal dystrophy central areolar",
          "choroidal dystrophy, central areolar, 1"
        ],
        "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 hereditary macular disorder, usually presenting between the ages of 30-60, characterized by a large area of atrophy in the center of the macula and the loss or absence of photoreceptors, retinal pigment epithelium and choriocapillaris in this area, resulting in a progressive decrease in visual acuity."
      },
      "child_count": 10,
      "reference_id": "MONDO:0008982"
    },
    {
      "id": 11006,
      "label": "ornithine aminotransferase deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4072,
        17673,
        19000,
        19748,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1415",
          "GARD:0006556",
          "MEDGEN:6695",
          "MESH:D015799",
          "NANDO:2200484",
          "NANDO:2200486",
          "NCIT:C84744",
          "OMIM:258870",
          "Orphanet:414",
          "UMLS:C0018425"
        ],
        "synonyms": [
          "GACR",
          "HOGA",
          "gyrate atrophy",
          "gyrate atrophy of choroid and retina with or without ornithinemia",
          "hoga",
          "hyperornithinemia",
          "hyperornithinemia-gyrate atrophy of choroid and retina syndrome",
          "ornithine aminotransferase deficiency",
          "Fuchs atrophia gyrata chorioideae et retinae",
          "Fuchs gyrate atrophy",
          "Fuchs gyrate atrophy of the choroid and retina",
          "Girate atrophy of the retina",
          "OAT deficiency",
          "OKT deficiency",
          "Oat deficiency",
          "Okt deficiency",
          "Ornithinemia",
          "gyrate atrophy of choroid and retina",
          "hyperornithinemia with gyrate atrophy of choroid and retina",
          "ornithine Keto acid aminotransferase deficiency",
          "ornithine ketoacid aminotransferase deficiency",
          "ornithine-Delta-aminotransferase deficiency"
        ],
        "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 very rare inherited retinal dystrophy characterized by progressive chorioretinal atrophy, myopia and early cataract."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009796"
    },
    {
      "id": 11711,
      "label": "choroideremia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2902,
        4072,
        19000,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9821",
          "GARD:0006061",
          "ICD10CM:H31.21",
          "ICD9:363.55",
          "MEDGEN:944",
          "MESH:D015794",
          "MedDRA:10008791",
          "NCIT:C34469",
          "NORD:932",
          "OMIM:303100",
          "Orphanet:180",
          "SCTID:75241009",
          "UMLS:C0008525",
          "icd11.foundation:217923263"
        ],
        "synonyms": [
          "CHM",
          "Tapetochoroidal dystrophy",
          "choroideremia",
          "progressive choroidal atrophy",
          "TCD",
          "Tapetochoroidal dystrophy, progressive",
          "choroidal sclerosis",
          "progressive tapetochoroidal dystrophy"
        ],
        "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": "Choroideremia (CHM) is an X-linked chorioretinal dystrophy characterized by progressive degeneration of the choroid, retinal pigment epithelium (RPE) and retina."
      },
      "child_count": 8,
      "reference_id": "MONDO:0010557"
    },
    {
      "id": 20462,
      "label": "choroid neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4072,
        20436,
        21330
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:3059",
          "NCIT:C2949",
          "UMLS:C0008523"
        ],
        "synonyms": [
          "choroid tumor",
          "choroid tumour",
          "choroidal neoplasm",
          "choroidal tumor",
          "choroidal tumour",
          "neoplasm of choroid",
          "neoplasm of optic choroid",
          "neoplasm of the choroid",
          "optic choroid neoplasm",
          "optic choroid neoplasm (disease)",
          "optic choroid tumor",
          "optic choroid tumour",
          "tumor of choroid",
          "tumor of optic choroid",
          "tumor of the choroid",
          "tumour of choroid",
          "tumour of optic choroid",
          "tumour of the choroid"
        ],
        "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 neoplasm (disease) that involves the optic choroid."
      },
      "child_count": 6,
      "reference_id": "MONDO:0021258"
    }
  ],
  "roots": [
    {
      "id": 4712,
      "label": "uveal disorder"
    },
    {
      "id": 7202,
      "label": "ocular vascular disorder"
    }
  ]
}