{
  "id": 3562,
  "label": "hypertrichosis of eyelid",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001334",
  "properties": {
    "xrefs": [
      "DOID:11669",
      "ICD10CM:H02.86",
      "ICD9:374.54",
      "MEDGEN:509853",
      "SCTID:79830009",
      "UMLS:C0155213",
      "icd11.foundation:1623148241"
    ],
    "synonyms": [
      "eyelid hypertrichosis (disease)",
      "hypertrichosis (disease) of eyelid"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A hypertrichosis (disease) that involves the eyelid."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 5315,
      "label": "eyelid disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2924,
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:530",
          "EFO:0009547",
          "ICD10CM:H00",
          "ICD9:374.89",
          "ICD9:374.9",
          "MEDGEN:41938",
          "MESH:D005141",
          "NCIT:C26768",
          "SCTID:60113004",
          "UMLS:C0015423"
        ],
        "synonyms": [
          "disease of eyelid",
          "disease or disorder of eyelid",
          "disorder of eyelid",
          "eyelid disease",
          "eyelid disease or disorder",
          "eyelid disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A disease involving the eyelid."
      },
      "child_count": 40,
      "reference_id": "MONDO:0003382"
    },
    {
      "id": 19135,
      "label": "hypertrichosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4924
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:420",
          "HP:0000998",
          "ICD10WHO:L68",
          "MEDGEN:43787",
          "MESH:D006983",
          "MedDRA:10020864",
          "Orphanet:79365",
          "SCTID:29966009",
          "UMLS:C0020555",
          "icd11.foundation:2042627850"
        ],
        "synonyms": [
          "hypertrichosis",
          "hypertrichosis (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Excessive hair growth anywhere on the body."
      },
      "child_count": 11,
      "reference_id": "MONDO:0019280"
    }
  ],
  "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"
    }
  ],
  "roots": [
    {
      "id": 5315,
      "label": "eyelid disorder"
    },
    {
      "id": 19135,
      "label": "hypertrichosis"
    }
  ]
}