{
  "id": 6376,
  "label": "retinoschisis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004579",
  "properties": {
    "xrefs": [
      "DOID:8465",
      "GARD:0027687",
      "ICD9:361.10",
      "MEDGEN:56292",
      "MESH:D041441",
      "NCIT:C85046",
      "SCTID:44268007",
      "UMLS:C0152439",
      "icd11.foundation:1118046584"
    ],
    "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": "An inherited or acquired disorder characterized by splitting of the retina into two layers. It results in loss of vision."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 6377,
      "label": "retinal degeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6979
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8466",
          "MEDGEN:48432",
          "MESH:D012162",
          "NCIT:C34979",
          "SCTID:95695004",
          "UMLS:C0035304"
        ],
        "synonyms": [
          "retina degeneration",
          "retina, Degeneration Of"
        ],
        "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": "Degeneration of the retina."
      },
      "child_count": 6,
      "reference_id": "MONDO:0004580"
    }
  ],
  "children": [
    {
      "id": 3653,
      "label": "bullous retinoschisis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6376
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12108",
          "GARD:0027579",
          "ICD9:361.12",
          "MEDGEN:576202",
          "SCTID:65545003",
          "UMLS:C0344289"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001435"
    },
    {
      "id": 6375,
      "label": "flat retinoschisis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6376
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8464",
          "GARD:0027686",
          "ICD9:361.11",
          "MEDGEN:509672",
          "SCTID:83405000",
          "UMLS:C0154817"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0004578"
    },
    {
      "id": 9681,
      "label": "retinoschisis, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2903,
        6376,
        19000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009144",
          "MEDGEN:357940",
          "MESH:C000598640",
          "OMIM:180270",
          "UMLS:C1867235"
        ],
        "synonyms": [
          "autosomal dominant retinoschisis",
          "retinoschisis, autosomal dominant",
          "retinoschisis autosomal dominant"
        ],
        "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": "Autosomal dominant form of retinoschisis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008382"
    },
    {
      "id": 11187,
      "label": "retinoschisis of fovea",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6376,
        19000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009143",
          "MEDGEN:340313",
          "MESH:C538369",
          "OMIM:268080",
          "UMLS:C1849397"
        ],
        "synonyms": [
          "retinoschisis of fovea",
          "familial foveal retinoschisis",
          "foveal retinoschisis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0009988"
    },
    {
      "id": 11865,
      "label": "X-linked retinoschisis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2902,
        6376,
        19000,
        19768
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060763",
          "GARD:0004690",
          "MEDGEN:811458",
          "NANDO:1200938",
          "NCIT:C75483",
          "NORD:1864",
          "OMIM:312700",
          "Orphanet:792",
          "SCTID:86923008",
          "UMLS:C3714753",
          "icd11.foundation:2074506458"
        ],
        "synonyms": [
          "X-linked juvenile retinoschisis",
          "X-linked juvenile retinoschisis type 1",
          "X-linked retinoschisis",
          "XLRS",
          "juvenile X-linked retinoschisis",
          "retinoschisis, X-linked",
          "retinoschisis, X-linked recessive",
          "RS",
          "RS1",
          "X-linked juvenile retinoschisis 1",
          "XJR",
          "XLRS1",
          "juvenile retinoschisis",
          "retinoschisis 1, X-linked, juvenile",
          "retinoschisis X-linked",
          "retinoschisis juvenile X chromosome-linked"
        ],
        "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": "A genetic ocular disease that is characterized by reduced visual acuity in males due to juvenile macular degeneration."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010725"
    }
  ],
  "roots": [
    {
      "id": 6377,
      "label": "retinal degeneration"
    }
  ]
}