{
  "id": 9253,
  "label": "lymphatic malformation 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007920",
  "properties": {
    "xrefs": [
      "DOID:0070213",
      "GARD:0003324",
      "MEDGEN:1648463",
      "MESH:C562467",
      "MedDRA:10027138",
      "OMIM:153200",
      "Orphanet:90186",
      "SCTID:400040008",
      "UMLS:C4746631"
    ],
    "synonyms": [
      "LMPH2",
      "Meige disease",
      "Meige lymphedema",
      "hereditary lymphedema type II",
      "late-onset primary lymphedema",
      "lymphedema hereditary type 2",
      "lymphedema praecox",
      "lymphedema, hereditary, II",
      "lymphedema, late-onset"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A frequent form of late-onset, primary lymphedema characterized by lower limb lymphedema typically developing during puberty."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2944,
      "label": "craniofacial dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2936
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050845",
          "GARD:0027532",
          "MEDGEN:868612",
          "UMLS:C4023011"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck."
      },
      "child_count": 1,
      "reference_id": "MONDO:0000486"
    },
    {
      "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"
    },
    {
      "id": 23165,
      "label": "neurovascular disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799,
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:857738",
          "NCIT:C117007",
          "UMLS:C3898144"
        ],
        "synonyms": [
          "disease of nervous system vasculature",
          "nervous system disorder of vasculature",
          "neurovascular disorder",
          "vasculature nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disorder of the nervous system related to a vascular etiology."
      },
      "child_count": 58,
      "reference_id": "MONDO:0043218"
    },
    {
      "id": 23452,
      "label": "inherited dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021630",
          "MEDGEN:1842468",
          "NANDO:1200511",
          "NCIT:C35527",
          "OMIMPS:128100",
          "Orphanet:391799",
          "UMLS:C5680022"
        ],
        "synonyms": [
          "familial dystonia",
          "hereditary dystonic disorder",
          "rare genetic dystonia",
          "rare genetic dystonic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of dystonic disorder that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 48,
      "reference_id": "MONDO:0044807"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2944,
      "label": "craniofacial dystonia"
    },
    {
      "id": 19154,
      "label": "lymphatic malformation"
    },
    {
      "id": 23165,
      "label": "neurovascular disorder"
    },
    {
      "id": 23452,
      "label": "inherited dystonia"
    }
  ]
}