{
  "id": 15974,
  "label": "glaucoma 3, primary congenital, E",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014998",
  "properties": {
    "xrefs": [
      "GARD:0018227",
      "MEDGEN:934606",
      "OMIM:617272",
      "UMLS:C4310639"
    ],
    "synonyms": [
      "GLC3E",
      "glaucoma 3, primary congenital, E",
      "glaucoma 3, primary congenital, E; GLC3E",
      "glaucoma 3, primary congenital, type E"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19827,
      "label": "congenital glaucoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18318
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11212",
          "GARD:0025157",
          "ICD9:743.2",
          "ICD9:743.20",
          "MEDGEN:42532",
          "MESH:D006871",
          "NCIT:C50648",
          "SCTID:204113001",
          "UMLS:C0020302"
        ],
        "synonyms": [
          "Buphthalmus",
          "buphthalmia",
          "buphthalmos",
          "hydrophthalmos",
          "primary congenital glaucoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A developmental glaucoma that results from the abnormal development of the aqueous drainage structure, characterized by an elevated intra-ocular pressure, enlargement of globe (buphthalmos), corneal edema and optic nerve cupping, and presenting clinically with the characteristic triad of epiphora, photophobia and blepharospasm."
      },
      "child_count": 4,
      "reference_id": "MONDO:0020366"
    },
    {
      "id": 24874,
      "label": "TEK-related primary glaucoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18318
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026473"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any primary hereditary glaucoma in which the cause of the disease is a mutation in the TEK gene."
      },
      "child_count": 1,
      "reference_id": "MONDO:0800182"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19827,
      "label": "congenital glaucoma"
    },
    {
      "id": 24874,
      "label": "TEK-related primary glaucoma"
    }
  ]
}