{
  "id": 3759,
  "label": "phacogenic glaucoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001554",
  "properties": {
    "xrefs": [
      "DOID:12571",
      "ICD9:365.59",
      "MEDGEN:543189",
      "SCTID:392300000",
      "UMLS:C0271142"
    ],
    "synonyms": [
      "phacomorphic glaucoma",
      "lens induced angle closure glaucoma",
      "lens swelling glaucoma"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Secondary glaucoma caused by either excessive size or spheric shape of the lens."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6774,
      "label": "glaucoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1686",
          "HP:0000501",
          "ICD10CM:H40",
          "ICD10CM:H40-H42",
          "ICD10WHO:H40",
          "ICD10WHO:H40-H42",
          "ICD9:365",
          "ICD9:365.89",
          "ICD9:365.9",
          "MEDGEN:42224",
          "MESH:D005901",
          "NCIT:C26782",
          "SCTID:23986001",
          "UMLS:C0017601",
          "icd11.foundation:499924848"
        ],
        "synonyms": [
          "glaucoma",
          "glaucoma (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Increased pressure in the eyeball due to obstruction of the outflow of aqueous humor."
      },
      "child_count": 11,
      "reference_id": "MONDO:0005041"
    }
  ],
  "children": [
    {
      "id": 3758,
      "label": "phacolytic glaucoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3759,
        8586
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12570",
          "ICD9:365.51",
          "MEDGEN:508901",
          "SCTID:32893002",
          "UMLS:C0152137",
          "icd11.foundation:1566213590"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An abnormal condition characterized by an acute autoimmune reaction of the eye. It is caused by hypersensitivity of the eye to the protein of the crystalline lens and commonly follows trauma to the crystalline lens or cataract surgery. Associated symptoms include swelling and inflammation of the eye, severe pain, and blurred vision. The substance of the lens is invaded by polymorphonuclear cells and mononuclear phagocytes. Accurate diagnosis must differentiate between this condition and infectious endophthalmitis. Therapy is supportive and commonly includes the administration of corticosteroids and atropine. Refractory cases may require surgical removal of the lens."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001553"
    },
    {
      "id": 9632,
      "label": "exfoliation syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3759,
        4370,
        4401,
        18318
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13641",
          "EFO:0004235",
          "GARD:0027786",
          "ICD9:365.52",
          "MEDGEN:60133",
          "MESH:D017889",
          "NCIT:C129025",
          "Orphanet:529819",
          "SCTID:111514006",
          "UMLS:C0206368"
        ],
        "synonyms": [
          "XFG",
          "XFS",
          "pseudoexfoliation glaucoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An autosomal dominant disorder caused by mutations in the LOXL1 gene, encoding lysyl oxidase homolog 1. The condition is characterized by abnormal fibrillar extracellular material in anterior segment tissues, and may lead to glaucoma."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008327"
    }
  ],
  "roots": [
    {
      "id": 6774,
      "label": "glaucoma"
    }
  ]
}