{
  "id": 6518,
  "label": "cleft lip",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004747",
  "properties": {
    "xrefs": [
      "DOID:9296",
      "HP:0410030",
      "ICD10CM:Q36",
      "ICD10WHO:Q36",
      "ICD9:749.1",
      "ICD9:749.10",
      "ICD9:749.11",
      "MEDGEN:1370297",
      "MESH:D002971",
      "NCIT:C87175",
      "SCTID:80281008",
      "UMLS:C4321245"
    ],
    "synonyms": [
      "cheiloschisis",
      "cleft lip",
      "cleft lip (disease)",
      "cleft lip, unilateral, complete",
      "labium leporinum"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A congenital abnormality consisting of one or more clefts (splits) in the upper lip, which may be accompanied by a cleft palate; it is the result of the failure of the embryonic parts of the lip to fuse."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 2863,
      "label": "orofacial cleft",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        21213
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050567",
          "MEDGEN:472000",
          "OMIMPS:119530",
          "SCTID:449790007",
          "UMLS:C3266076"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disorder of facial skeleton that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development."
      },
      "child_count": 32,
      "reference_id": "MONDO:0000358"
    }
  ],
  "children": [
    {
      "id": 8891,
      "label": "Rapp-Hodgkin syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2903,
        6518,
        16697,
        19138,
        29233
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060330",
          "GARD:0005690",
          "MEDGEN:315656",
          "MESH:C535289",
          "OMIM:129400",
          "Orphanet:3022",
          "SCTID:7731005",
          "UMLS:C1785148",
          "icd11.foundation:1455333054"
        ],
        "synonyms": [
          "Rapp-Hodgkin syndrome",
          "OFC8, included",
          "RHS",
          "Rapp-Hodgkin ectodermal dysplasia syndrome",
          "cleft lip with or without cleft palate, nonsyndromic, 8",
          "ectodermal dysplasia, anhidrotic, with cleft Lip/palate",
          "ectodermal dysplasia, anhidrotic, with cleft lip-palate",
          "orofacial cleft 8"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A form of ectodermal dysplasia characterized by the association of anhidrotic ectodermal dysplasia with cleft lip/palate."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007508"
    },
    {
      "id": 16679,
      "label": "isolated cleft lip",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6518,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017091",
          "MEDGEN:40327",
          "MedDRA:10009259",
          "Orphanet:199302",
          "UMLS:C0008924",
          "icd11.foundation:172183323"
        ],
        "synonyms": [
          "isolated cleft lip (disease)",
          "nonsyndromic cleft lip (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Isolated cleft lip is a fissure type embryopathy extending from the upper lip to the nasal base."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016043"
    },
    {
      "id": 21242,
      "label": "Kuster syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        6518,
        16697
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003152",
          "MEDGEN:419150",
          "MESH:C538126",
          "UMLS:C2931741"
        ],
        "synonyms": [
          "cleft lip and palate, lower lip pits, and limb deficiency defects",
          "cleft lip palate lip pits limb deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0023581"
    }
  ],
  "roots": [
    {
      "id": 2863,
      "label": "orofacial cleft"
    }
  ]
}