{
  "id": 22255,
  "label": "hennekam lymphangiectasia-lymphedema syndrome 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0032564",
  "properties": {
    "xrefs": [
      "GARD:0016296",
      "MEDGEN:1648368",
      "OMIM:618154",
      "UMLS:C4748408"
    ],
    "synonyms": [
      "HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3",
      "HKLLS3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16822,
      "label": "Hennekam syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        16087,
        19154
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060366",
          "GARD:0003318",
          "ICD9:457.1",
          "MEDGEN:137946",
          "OMIMPS:235510",
          "Orphanet:2136",
          "SCTID:234146006",
          "UMLS:C0340834",
          "icd11.foundation:162216708"
        ],
        "synonyms": [
          "Hennekam lymphangiectasia lymphedema syndrome",
          "Hennekam lymphangiectasia-lymphedema syndrome",
          "lymphedema-lymphangiectasia-intellectual disability syndrome",
          "intestinal lymphagiectasia lymphedema intellectual deficit syndrome",
          "lymphangiectasies and lymphedema Hennekam type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Hennekam syndrome is characterized by the association of lymphoedema, intestinal lymphangiectasia, intellectual deficit and facial dysmorphism."
      },
      "child_count": 9,
      "reference_id": "MONDO:0016256"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16822,
      "label": "Hennekam syndrome"
    }
  ]
}