{
  "id": 16805,
  "label": "infantile hemangioma of rare localization",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016223",
  "properties": {
    "xrefs": [
      "GARD:0020453",
      "MEDGEN:825458",
      "Orphanet:210589",
      "SCTID:703270004",
      "UMLS:C3839613"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 7994,
      "label": "hemangioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21322
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:255",
          "EFO:1000635",
          "HP:0001028",
          "ICD10CM:D18.0",
          "ICD9:228.0",
          "ICD9:228.00",
          "ICD9:228.09",
          "ICDO:9120/0",
          "MEDGEN:5477",
          "MESH:D006391",
          "NCIT:C3085",
          "ONCOTREE:HEMA",
          "SCTID:400210000",
          "UMLS:C0018916"
        ],
        "synonyms": [
          "benign hemangioma",
          "hemangioma",
          "hemangioma, benign",
          "angioma",
          "benign angioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A benign vascular lesion characterized by the formation of capillary-sized or cavernous vascular channels."
      },
      "child_count": 28,
      "reference_id": "MONDO:0006500"
    }
  ],
  "children": [
    {
      "id": 12831,
      "label": "primary intraosseous venous malformation",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        16805
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016961",
          "MEDGEN:376071",
          "MESH:C564648",
          "OMIM:606893",
          "Orphanet:140436",
          "SCTID:764100007",
          "UMLS:C1847197"
        ],
        "synonyms": [
          "intraosseous hemangioma",
          "osseous venous malformation",
          "hemangioma, intraosseous",
          "vascular malformation osseous",
          "vascular malformation, primary intraosseous"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Primary intraosseous venous malformation is a rare, genetic vascular anomaly characterized by severe blood vessel expansion (most frequently within the craniofacial bones) with painless bone enlargement (usually of mandibule, maxilla and/or orbital, nasal, and frontal bones), typically resulting in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos, loss of vision, nausea, and vomiting."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011744"
    },
    {
      "id": 16194,
      "label": "laryngotracheal angioma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7231,
        16805,
        21538
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019893",
          "ICD9:228.09",
          "MEDGEN:825419",
          "NCIT:C99086",
          "Orphanet:137935",
          "SCTID:703199001",
          "UMLS:C3839574"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015317"
    },
    {
      "id": 26064,
      "label": "isolated segmental infantile hemangioma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16805
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027195",
          "MEDGEN:1863691",
          "Orphanet:675380",
          "UMLS:C5925079"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0971133"
    }
  ],
  "roots": [
    {
      "id": 7994,
      "label": "hemangioma"
    }
  ]
}