{
  "id": 9252,
  "label": "lymphatic malformation 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007919",
  "properties": {
    "xrefs": [
      "DOID:0070210",
      "DOID:0070212",
      "GARD:0003328",
      "MEDGEN:309963",
      "OMIM:153100",
      "Orphanet:79452",
      "SCTID:399889006",
      "UMLS:C1704423"
    ],
    "synonyms": [
      "FLT4 hereditary lymphedema",
      "LMPH1A",
      "Milroy disease",
      "Nonne-Milroy disease",
      "Nonne-Milroy lymphedema",
      "Nonne-Milroy syndrome",
      "Nonne’s syndrome",
      "congenital hereditary lymphedema",
      "early onset lymphedema",
      "hereditary lymphedema 1",
      "hereditary lymphedema caused by mutation in FLT4",
      "hereditary lymphedema type I",
      "lymphedema, early-onset",
      "lymphedema, hereditary, 1A",
      "lymphedema, hereditary, type 1A",
      "primary congenital lymphedema"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "Any hereditary lymphedema in which the cause of the disease is a mutation in the FLT4 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19154,
      "label": "lymphatic malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7065,
        19049
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050580",
          "GARD:0013057",
          "ICD10CM:Q82.0",
          "ICD9:757.0",
          "MEDGEN:140763",
          "OMIMPS:153100",
          "SCTID:254199006",
          "UMLS:C0398368"
        ],
        "synonyms": [
          "hereditary lymphedema",
          "lymphedema, hereditary"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Primary lymphedema is caused by anatomic or functional defects in the lymphatic system, resulting in chronic swelling of body parts and lymphatic-system malformation."
      },
      "child_count": 84,
      "reference_id": "MONDO:0019313"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19154,
      "label": "lymphatic malformation"
    }
  ]
}