{
  "id": 19756,
  "label": "congenital ectropion",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020161",
  "properties": {
    "xrefs": [
      "GARD:0019502",
      "ICD10CM:Q10.1",
      "MEDGEN:540010",
      "Orphanet:98570",
      "SCTID:26590002",
      "UMLS:C0266578",
      "icd11.foundation:945558601"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 4190,
      "label": "ectropion",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5315
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1570",
          "HP:0000656",
          "ICD10CM:H02.1",
          "ICD9:374.1",
          "ICD9:374.10",
          "MEDGEN:4448",
          "MESH:D004483",
          "SCTID:62909004",
          "UMLS:C0013592"
        ],
        "synonyms": [
          "ectropion",
          "ectropion (disease)",
          "ectropion of eyelid"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed)"
      },
      "child_count": 5,
      "reference_id": "MONDO:0002043"
    }
  ],
  "children": [
    {
      "id": 8734,
      "label": "blepharocheilodontic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        16089,
        19138,
        19756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080344",
          "GARD:0002071",
          "MEDGEN:349302",
          "MESH:C536188",
          "OMIMPS:119580",
          "Orphanet:1997",
          "SCTID:717911008",
          "UMLS:C1861536",
          "icd11.foundation:755252042"
        ],
        "synonyms": [
          "BCD syndrome",
          "Elsching syndrome",
          "blepharo-cheilo-odontic syndrome",
          "blepharocheilodontic syndrome",
          "clefting-ectropion-conical teeth syndrome",
          "ectropion inferior-cleft lip and or palate syndrome",
          "ectropion inferior-cleft lip and/or palate syndrome",
          "lagophthalmia-cleft lip and palate syndrome",
          "BCDS",
          "BCDS1",
          "Elschnig syndrome",
          "blepharo-cheilo-dontic syndrome",
          "blepharocheilodontic syndrome 1",
          "clefting, ectropion, and conical teeth",
          "ectropion inferior cleft lip and or palate",
          "ectropion, inferior, with cleft lip and/or palate",
          "lagophthalmia with bilateral cleft lip and palate"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An ectodermal dysplasia syndrome characterized by the association of abnormalities of the eyelids, lips, and teeth."
      },
      "child_count": 12,
      "reference_id": "MONDO:0007339"
    },
    {
      "id": 19922,
      "label": "isolated congenital ectropion",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019673",
          "MEDGEN:1842688",
          "Orphanet:99171",
          "UMLS:C5681630"
        ],
        "synonyms": [
          "nonsyndromic congenital ectropion"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A congenital ectropion that is not part of a larger syndrome."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020463"
    },
    {
      "id": 19923,
      "label": "euryblepharon",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019674",
          "MEDGEN:724511",
          "Orphanet:99172",
          "SCTID:400954002",
          "UMLS:C1303001",
          "icd11.foundation:2086603843"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Euryblepharon is a rare congenital eyelid anomaly of unknown etiology characterized by the bilateral horizontal enlargement of the palpebral fissure with vertically shortened eyelids, lateral canthus malpositioning and lateral ectropion. It may be isolated or associated with other ocular anomalies (e.g. strabismus or telecanthus) or systemic anomalies (e.g. blepharo-cheilo-odontic syndrome). In severe cases, it may result in lagophthalmos and exposure keratopathy, requiring surgical treatment."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020464"
    }
  ],
  "roots": [
    {
      "id": 4190,
      "label": "ectropion"
    }
  ]
}