{
  "id": 9216,
  "label": "congenital laryngeal web",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007880",
  "properties": {
    "xrefs": [
      "GARD:0016596",
      "MEDGEN:372058",
      "MESH:C537676",
      "MESH:C563636",
      "MedDRA:10023871",
      "NCIT:C98970",
      "OMIM:150360",
      "Orphanet:2374",
      "SCTID:444921008",
      "UMLS:C1835494",
      "icd11.foundation:1641764672"
    ],
    "synonyms": [
      "Laryngeal web",
      "gay Feinmesser Cohen syndrome",
      "glottic web, congenital anterior",
      "laryngeal web, congenital heart disease and low stature",
      "laryngeal web, familial",
      "subglottic Bar",
      "subglottic bar, congenital heart disease and low stature",
      "subglottic web"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "Congenital laryngeal web is a rare malformation consisting of a membrane-like structure that extends across the laryngeal lumen close to the level of the vocal cords."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 6195,
      "label": "laryngeal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6623
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:786",
          "EFO:0009673",
          "ICD9:478.70",
          "MEDGEN:7268",
          "MESH:D007818",
          "NCIT:C26810",
          "SCTID:60600009",
          "UMLS:C0023051"
        ],
        "synonyms": [
          "disease of larynx",
          "disease or disorder of larynx",
          "disorder of larynx",
          "disorder of the larynx",
          "laryngeal disease",
          "laryngeal disorder",
          "larynx disease",
          "larynx disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the larynx. Representative examples include laryngitis, vocal cord polyp, squamous papilloma, and carcinoma."
      },
      "child_count": 20,
      "reference_id": "MONDO:0004382"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 6195,
      "label": "laryngeal disorder"
    }
  ]
}