{
  "id": 9184,
  "label": "autosomal dominant keratitis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007848",
  "properties": {
    "xrefs": [
      "DOID:0111383",
      "GARD:0003089",
      "MEDGEN:332039",
      "MESH:C537022",
      "OMIM:148190",
      "Orphanet:2334",
      "SCTID:715339004",
      "UMLS:C1835698",
      "icd11.foundation:682617640"
    ],
    "synonyms": [
      "hereditary keratitis",
      "keratitis, autosomal dominant",
      "dominantly inherited keratitis",
      "keratitis, hereditary"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Hereditary keratitis is characterized by opacification and vascularisation of the cornea, often associated with macula hypoplasia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 5071,
      "label": "keratitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4677",
          "EFO:0009449",
          "ICD10CM:H16",
          "ICD10WHO:H16",
          "ICD9:370",
          "ICD9:370.8",
          "ICD9:370.9",
          "MEDGEN:44013",
          "MESH:D007634",
          "NCIT:C26805",
          "SCTID:5888003",
          "UMLS:C0022568"
        ],
        "synonyms": [
          "cornea inflammation",
          "inflammation of cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A corneal disease that is characterized by inflammation of the cornea."
      },
      "child_count": 22,
      "reference_id": "MONDO:0003085"
    },
    {
      "id": 18261,
      "label": "corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3211
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2566",
          "GARD:0027867",
          "HP:0001131",
          "ICD9:371.5",
          "ICD9:371.50",
          "MEDGEN:3619",
          "MESH:D003317",
          "MedDRA:10011005",
          "NCIT:C34513",
          "Orphanet:34533",
          "SCTID:5587004",
          "UMLS:C0010036",
          "icd11.foundation:1291475891"
        ],
        "synonyms": [
          "corneal dystrophy",
          "corneal dystrophy (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value."
      },
      "child_count": 13,
      "reference_id": "MONDO:0018102"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 5071,
      "label": "keratitis"
    },
    {
      "id": 18261,
      "label": "corneal dystrophy"
    }
  ]
}