{
  "id": 8529,
  "label": "hereditary neurocutaneous angioma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007116",
  "properties": {
    "xrefs": [
      "GARD:0000676",
      "MEDGEN:226898",
      "OMIM:106070",
      "Orphanet:1062",
      "UMLS:C1275084",
      "icd11.foundation:182579434"
    ],
    "synonyms": [
      "hereditary neurocutaneous angioma",
      "angioma hereditary neurocutaneous",
      "angioma, hereditary neurocutaneous",
      "hemangiomatosis, disseminated",
      "hereditary neurocutaneous malformation",
      "spinal arterial Venous malformations with cutaneous hemangiomas"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Hereditary neurocutaneous angioma is characterized by the association of cerebral and cutaneous angiomatous lesions. It has been described in less than 10 families. Clinical manifestations of the cerebral lesions include epilepsy, cerebral hemorrhage, and focal neurological deficit. Transmission is autosomal dominant."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19507,
      "label": "developmental defect during embryogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:759.7",
          "MEDGEN:1825997",
          "NCIT:C99267",
          "Orphanet:93890",
          "SCTID:400038003",
          "UMLS:C5680284"
        ],
        "synonyms": [
          "congenital malformation syndrome",
          "developmental defect during embryogenesis",
          "disorder of embryonic morphogenesis",
          "embryonic morphogenesis disease",
          "malformation syndrome",
          "rare developmental defect during embryogenesis"
        ],
        "definition": "A disease that has its basis in the disruption of embryonic morphogenesis."
      },
      "child_count": 52,
      "reference_id": "MONDO:0019755"
    },
    {
      "id": 21330,
      "label": "vascular neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21585
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:129202",
          "NCIT:C7388",
          "UMLS:C0282607"
        ],
        "synonyms": [
          "neoplasm of vascular system",
          "neoplasm of vascular tissue",
          "neoplasms, vascular",
          "tumor of vascular system",
          "tumor of vascular tissue",
          "tumors, vascular",
          "tumour of vascular system",
          "tumour of vascular tissue",
          "vascular neoplasm",
          "vascular neoplasms",
          "vascular system neoplasm",
          "vascular system neoplasm (disease)",
          "vascular system tumor",
          "vascular system tumour",
          "vascular tissue neoplasm",
          "vascular tissue tumor",
          "vascular tissue tumour",
          "vascular tumor",
          "vascular tumors",
          "vascular tumour",
          "vascular tumours"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A benign, intermediate, or malignant neoplasm arising from vascular tissue including arteries, veins, venous sinuses, lymphatic vessels, arterioles and capillaries. It may occur in essentially any body location and is characterized by the presence of vascular channel formation and endothelial cells."
      },
      "child_count": 16,
      "reference_id": "MONDO:0024296"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19507,
      "label": "developmental defect during embryogenesis"
    },
    {
      "id": 21330,
      "label": "vascular neoplasm"
    }
  ]
}