{
  "id": 15426,
  "label": "nanophthalmos 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014426",
  "properties": {
    "xrefs": [
      "GARD:0018629",
      "MEDGEN:863285",
      "OMIM:615972",
      "UMLS:C4014848"
    ],
    "synonyms": [
      "TMEM98 nanophthalmia",
      "nanophthalmia caused by mutation in TMEM98",
      "nanophthalmos 4",
      "nanophthalmos type 4",
      "NNO4",
      "Nanophthalmia 4"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Any nanophthalmia in which the cause of the disease is a mutation in the TMEM98 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7169,
      "label": "nanophthalmia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        17209,
        20367
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080634",
          "GARD:0016637",
          "MEDGEN:901455",
          "OMIMPS:600165",
          "Orphanet:35612",
          "SCTID:716775009",
          "UMLS:C4274282"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Nanophthalmia is a severe form of microphthalmia characterized by a small eye with a short axial length, severe hyperopia, an elevated lens/eye ratio, and a high incidence of angle-closure glaucoma."
      },
      "child_count": 12,
      "reference_id": "MONDO:0005514"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7169,
      "label": "nanophthalmia"
    }
  ]
}