{
  "id": 4014,
  "label": "visual pathway disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001834",
  "properties": {
    "xrefs": [
      "DOID:1393",
      "ICD10CM:H47.9",
      "MEDGEN:57831",
      "NCIT:C35342",
      "SCTID:54767005",
      "SCTID:95776004",
      "UMLS:C0155287"
    ],
    "synonyms": [
      "disease of optic tract",
      "disease or disorder of optic tract",
      "disorder of optic tract",
      "optic tract disease",
      "optic tract disease or disorder",
      "visual pathway disorder",
      "optic tract disorder"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A disorder of the neural pathway from the optic nerve to the visual cortex."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 7209,
      "label": "brain disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:936",
          "EFO:0005774",
          "ICD9:348.3",
          "ICD9:348.30",
          "ICD9:348.8",
          "ICD9:348.9",
          "MEDGEN:14214",
          "MESH:D001927",
          "NCIT:C96413",
          "SCTID:81308009",
          "UMLS:C0006111"
        ],
        "synonyms": [
          "brain disease",
          "brain disease or disorder",
          "disease of brain",
          "disease or disorder of brain",
          "disorder of brain",
          "encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease affecting the brain or part of the brain."
      },
      "child_count": 71,
      "reference_id": "MONDO:0005560"
    },
    {
      "id": 20325,
      "label": "vision disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21402,
        21415
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:12103",
          "MESH:D014786",
          "MedDRA:10047518",
          "NCIT:C35126",
          "SCTID:95677002",
          "UMLS:C0042790"
        ],
        "synonyms": [
          "disorder of visual system",
          "visual system disorder",
          "disorder of vision",
          "vision disorder",
          "visual disorder",
          "visual Field disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any impairment to the vision."
      },
      "child_count": 14,
      "reference_id": "MONDO:0021084"
    }
  ],
  "children": [
    {
      "id": 5476,
      "label": "retinal nerve fiber layer disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4014,
        6979
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5678",
          "ICD9:362.85",
          "MEDGEN:784046",
          "SCTID:193428001",
          "UMLS:C3665426"
        ],
        "synonyms": [
          "disease of nerve fiber layer of retina",
          "disease of nerve fibre layer of retina",
          "disease or disorder of nerve fiber layer of retina",
          "disease or disorder of nerve fibre layer of retina",
          "disorder of nerve fiber layer of retina",
          "disorder of nerve fibre layer of retina",
          "nerve fiber layer of retina disease",
          "nerve fiber layer of retina disease or disorder",
          "nerve fibre layer of retina disease",
          "nerve fibre layer of retina disease or disorder",
          "retinal nerve fiber bundle defects",
          "retinal nerve fibre bundle defects",
          "retinal nerve fibre bundle deficiency",
          "nerve fiber bundle defect",
          "nerve fibre bundle defect"
        ],
        "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 disease that involves the nerve fiber layer of retina."
      },
      "child_count": 2,
      "reference_id": "MONDO:0003579"
    },
    {
      "id": 5479,
      "label": "visual cortex disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4014,
        23499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5691",
          "GARD:0027642",
          "ICD10CM:H47.6",
          "ICD9:377.7",
          "MEDGEN:66699",
          "NCIT:C35275",
          "Orphanet:447788",
          "SCTID:128329001",
          "UMLS:C0234398"
        ],
        "synonyms": [
          "disease of visual cortex",
          "disease or disorder of visual cortex",
          "disorder of visual cortex",
          "visual cortex disease",
          "visual cortex disease or disorder",
          "visual cortex disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A disease involving the visual cortex."
      },
      "child_count": 4,
      "reference_id": "MONDO:0003584"
    },
    {
      "id": 8747,
      "label": "coloboma of optic nerve",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3690,
        4014,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11975",
          "GARD:0001438",
          "HP:0000588",
          "ICD9:377.23",
          "MEDGEN:57832",
          "MESH:C535970",
          "OMIM:120430",
          "Orphanet:98947",
          "SCTID:17541006",
          "UMLS:C0155299",
          "icd11.foundation:592278969"
        ],
        "synonyms": [
          "coloboma of optic nerve (disease)",
          "coloboma of optic papilla",
          "optic nerve coloboma",
          "congenital coloboma of the optic nerve",
          "coloboma of optic disc",
          "morning glory Disc anomaly",
          "optic nerve head pits, bilateral congenital"
        ],
        "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": 3,
      "reference_id": "MONDO:0007354"
    },
    {
      "id": 16766,
      "label": "optic pathway glioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4014,
        17197,
        20287,
        20429
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004107",
          "MEDGEN:162950",
          "NCIT:C8567",
          "Orphanet:2086",
          "UMLS:C0796418",
          "icd11.foundation:1000103370"
        ],
        "synonyms": [
          "glioma of optic tract",
          "glioma of the optic tract",
          "glioma of the visual pathway",
          "glioma of visual pathway",
          "optic pathway glioma",
          "optic tract glioma",
          "visual pathway glioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Optic pathway glioma (OPG) is a benign tumor that develop along the optic nerve (chiasm, tracts, and radiations) characterized by impairment or loss of vision and may be accompanied by diencephalic symptoms such as reduced growth and alteration in sleeping patterns. OPG are often linked to neurofibromatosis type 1 (NF1)."
      },
      "child_count": 8,
      "reference_id": "MONDO:0016167"
    },
    {
      "id": 21556,
      "label": "optic tract meningioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4014,
        17113,
        20429
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025444",
          "MEDGEN:234991",
          "NCIT:C5587",
          "UMLS:C1336972"
        ],
        "synonyms": [
          "meningioma (disease) of optic tract",
          "meningioma of optic tract",
          "meningioma of the optic tract",
          "meningioma of the visual pathway",
          "meningioma of visual pathway",
          "optic tract meningioma",
          "optic tract meningioma (disease)",
          "visual pathway meningioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A meningioma that affects the visual pathway."
      },
      "child_count": 6,
      "reference_id": "MONDO:0024648"
    }
  ],
  "roots": [
    {
      "id": 7209,
      "label": "brain disorder"
    },
    {
      "id": 20325,
      "label": "vision disorder"
    }
  ]
}