{
  "id": 16257,
  "label": "cerebrofacial arteriovenous metameric syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015405",
  "properties": {
    "xrefs": [
      "GARD:0012662",
      "MEDGEN:825110",
      "Orphanet:141189",
      "SCTID:703266007",
      "UMLS:C3839265",
      "icd11.foundation:1402414905"
    ],
    "synonyms": [
      "CAMS"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A disorder characterized by vascular malformations that encompasses a spectrum of phenotypic expression involving arteriovenous malformations (AVMs) of the cerebral, orbital, and facial region."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 3493,
      "label": "arteriovenous hemangioma/malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7994
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "CSP:0571-2717",
          "DOID:11294",
          "HP:0100026",
          "ICDO:9123/0",
          "MEDGEN:137780",
          "MESH:D001165",
          "NCIT:C2882",
          "SCTID:233982006",
          "UMLS:C0334533"
        ],
        "synonyms": [
          "arteriovenous angioma",
          "arteriovenous hemangioma",
          "arteriovenous hemangioma/malformation",
          "racemose aneurysm (morphologic abnormality)",
          "racemose hemangioma (morphologic abnormality)",
          "arteriovenous malformation",
          "cirsoid aneurysm"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A benign vascular lesion characterized by the presence of a complex network of communicating arterial and venous vascular structures."
      },
      "child_count": 7,
      "reference_id": "MONDO:0001256"
    }
  ],
  "children": [
    {
      "id": 16258,
      "label": "cerebrofacial arteriovenous metameric syndrome type 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16257
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019959",
          "MEDGEN:825947",
          "Orphanet:141194",
          "SCTID:703267003",
          "UMLS:C3840102",
          "icd11.foundation:796738143"
        ],
        "synonyms": [
          "CAMS1"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015406"
    },
    {
      "id": 16259,
      "label": "cerebrofacial arteriovenous metameric syndrome type 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16257
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019960",
          "MEDGEN:824537",
          "Orphanet:141199",
          "SCTID:703268008",
          "UMLS:C3838691",
          "icd11.foundation:1048965538"
        ],
        "synonyms": [
          "CAMS3"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015407"
    },
    {
      "id": 18820,
      "label": "Wyburn-Mason syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5091,
        16257,
        19142,
        20682,
        23107,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0007900",
          "MEDGEN:120534",
          "MESH:C536752",
          "MedDRA:10048661",
          "NORD:1863",
          "Orphanet:53719",
          "SCTID:6729006",
          "UMLS:C0265321"
        ],
        "synonyms": [
          "CAMS2",
          "Cerebrofacial arteriovenous metameric syndrome type 2",
          "bonnet-Dechaume-Blanc syndrome",
          "Wyburn Mason syndrome",
          "Wyburn Mason's syndrome",
          "arteriovenous aneurysm of mid-brain and retina, facial nevi and mental changes",
          "bonnet-Decaume-Blanc syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Wyburn-Mason syndrome or Bonnet-Dechaume-Blanc syndrome is characterized by the association of arteriovenous malformations of the maxilla, retina, optic nerve, thalamus, hypothalamus and cerebral cortex."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018892"
    }
  ],
  "roots": [
    {
      "id": 3493,
      "label": "arteriovenous hemangioma/malformation"
    }
  ]
}