{
  "id": 9686,
  "label": "ring dermoid of cornea",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008387",
  "properties": {
    "xrefs": [
      "DOID:0111548",
      "GARD:0009696",
      "MEDGEN:357922",
      "MESH:C535684",
      "OMIM:180550",
      "Orphanet:91481",
      "SCTID:723499000",
      "UMLS:C1867155",
      "icd11.foundation:271430543"
    ],
    "synonyms": [
      "Ring dermoid syndrome",
      "ring dermoid of cornea",
      "RDC",
      "RING dermoid of cornea",
      "bilateral, annular limbal dermoids with corneal and conjunctival extension"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Ring dermoid of cornea is characterized by annular limbal dermoids (growths with a skin-like structure) with corneal and conjunctival extension. Less than 30 cases have been described. Transmission is autosomal dominant and mutations in the PITX2 gene have been suggested as a potential cause of the condition."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 20431,
      "label": "eye neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019,
        7231
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0003824",
          "ICD10CM:C69-C72",
          "MEDGEN:5095",
          "NCIT:C3030",
          "ONCOTREE:EYE",
          "UMLS:C0015414"
        ],
        "synonyms": [
          "eye neoplasm (disease)",
          "eye tumor",
          "eye tumour",
          "eyeball of camera-type eye neoplasm",
          "eyeball of camera-type eye tumor",
          "eyeball of camera-type eye tumour",
          "neoplasm of eye",
          "neoplasm of eyeball of camera-type eye",
          "neoplasm of the eye",
          "ocular neoplasm",
          "ocular tumor",
          "ocular tumour",
          "tumor of eye",
          "tumor of eyeball of camera-type eye",
          "tumor of the eye",
          "tumour of eye",
          "tumour of eyeball of camera-type eye",
          "tumour of the eye"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A neoplasm (disease) that involves the eye."
      },
      "child_count": 26,
      "reference_id": "MONDO:0021220"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 20431,
      "label": "eye neoplasm"
    }
  ]
}