{
  "id": 19755,
  "label": "congenital entropion",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020159",
  "properties": {
    "xrefs": [
      "ICD10CM:Q10.2",
      "MEDGEN:540011",
      "MedDRA:10014923",
      "Orphanet:98568",
      "SCTID:20392000",
      "UMLS:C0266579"
    ],
    "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": 3727,
      "label": "entropion",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5315
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12397",
          "HP:0000621",
          "ICD9:374.00",
          "MEDGEN:41813",
          "MESH:D004774",
          "SCTID:33168009",
          "UMLS:C0014390"
        ],
        "synonyms": [
          "entropion",
          "entropion (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The turning inward (inversion) of the edge of the eyelid, with the tarsal cartilage turned inward toward the eyeball. (Dorland, 27th ed)"
      },
      "child_count": 5,
      "reference_id": "MONDO:0001519"
    }
  ],
  "children": [
    {
      "id": 10118,
      "label": "Barber-Say syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3562,
        16089,
        19138,
        19755
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060549",
          "GARD:0000819",
          "MEDGEN:230818",
          "MESH:C537908",
          "NORD:875",
          "OMIM:209885",
          "Orphanet:1231",
          "SCTID:408537003",
          "UMLS:C1319466",
          "icd11.foundation:37248895"
        ],
        "synonyms": [
          "Barber-Say syndrome",
          "Brown Séquard Syndrome",
          "hypertrichosis-atrophic skin-ectropion-macrostomia syndrome",
          "BARBER-SAY syndrome",
          "BBRSAY",
          "Barber Say syndrome",
          "Bss",
          "hypertrichosis atrophic skin ectropion macrostomia",
          "hypertrichosis, atrophic skin, ectropion, and macrostomia"
        ],
        "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": "Barber Say syndrome (BSS) is a rare ectodermal dysplasia with neonatal onset characterized by congenital generalized hypertrichosis, atrophic skin, ectropion and microstomia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008853"
    },
    {
      "id": 19921,
      "label": "tarsal kink syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19755
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019672",
          "MEDGEN:724510",
          "Orphanet:99170",
          "UMLS:C1303000"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Tarsal kink syndrome is a rare congenital malformation of the tarsus that causes entropion characterized by blepharospasm and absence of an upper eyelid fold that may lead to corneal ulceration caused by the folded edge of the upper tarsus or the inturned eyelashes if not corrected by surgery."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020462"
    },
    {
      "id": 22788,
      "label": "isolated congenital entropion",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19755
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022123",
          "Orphanet:519386",
          "icd11.foundation:1290880184"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A rare eyelid malposition disorder characterized by congenital abnormal inversion of the eyelid towards the globe, potentially causing mechanical irritation of the ocular surface by the eyelashes, which may lead to corneal abrasion and scarring with visual impairment. Typical initial symptoms are foreign body sensation, redness, tearing, and ocular discharge."
      },
      "child_count": 0,
      "reference_id": "MONDO:0034971"
    }
  ],
  "roots": [
    {
      "id": 3727,
      "label": "entropion"
    }
  ]
}