{
  "id": 12313,
  "label": "capillary infantile hemangioma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011191",
  "properties": {
    "xrefs": [
      "MEDGEN:355573",
      "MESH:C535860",
      "NCIT:C6645",
      "OMIM:602089",
      "Orphanet:464293",
      "Orphanet:91415",
      "UMLS:C1865871"
    ],
    "synonyms": [
      "HCI",
      "hemangioma, capillary infantile",
      "hemangioma, capillary infantile, somatic",
      "hemangioma, hereditary capillary",
      "hereditary capillary infantile hemangioma"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Capillary hemangiomas are benign, highly proliferative lesions involving aberrant localized growth of capillary endothelium. They are the most common tumor of infancy, occurring in up to 10% of all births. Hemangiomas tend to appear shortly after birth and show rapid neonatal growth for up to 12 months characterized by endothelial hypercellularity and increased numbers of mast cells. This phase is followed by slow involution at a rate of about 10% per year and replacement by fibrofatty stroma. Hemangiomas are classified as distinct from vascular malformations, in that the latter are present from birth, tend to grow with the individual, do not regress, and show normal rates of endothelial cell turnover."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4497,
      "label": "capillary hemangioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7994
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2725",
          "ICDO:9131/0",
          "MEDGEN:64643",
          "MESH:D018324",
          "NCIT:C7457",
          "SCTID:56975005",
          "UMLS:C0206733"
        ],
        "synonyms": [
          "capillary angioma",
          "capillary hemangioma",
          "capillary hemangioma (morphologic abnormality)",
          "cellular hemangioma of infancy",
          "cellular hemangioma of infancy (strawberry nevus)",
          "infantile hemangioma",
          "juvenile hemangioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A common hemangioma characterized by the presence of capillary-sized vascular channels without prominent epithelioid endothelial cells."
      },
      "child_count": 6,
      "reference_id": "MONDO:0002407"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4497,
      "label": "capillary hemangioma"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}