{
  "id": 18820,
  "label": "Wyburn-Mason syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018892",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5091,
      "label": "skin hemangioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7994,
        20564
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:471",
          "MEDGEN:151951",
          "NCIT:C4905",
          "SCTID:93471006",
          "UMLS:C0687140"
        ],
        "synonyms": [
          "angioma of skin",
          "angioma of the skin",
          "hemangioma of skin",
          "hemangioma of the skin",
          "hemangioma of zone of skin",
          "skin angioma",
          "skin hemangioma",
          "zone of skin hemangioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A hemangioma arising from the skin."
      },
      "child_count": 20,
      "reference_id": "MONDO:0003110"
    },
    {
      "id": 16257,
      "label": "cerebrofacial arteriovenous metameric syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3493
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 3,
      "reference_id": "MONDO:0015405"
    },
    {
      "id": 19142,
      "label": "skin vascular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820,
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9540",
          "ICD9:709.1",
          "MEDGEN:102473",
          "MESH:D017445",
          "MedDRA:10062171",
          "NCIT:C35254",
          "Orphanet:79379",
          "SCTID:11263005",
          "UMLS:C0162819"
        ],
        "synonyms": [
          "skin vascular disorder",
          "superficial vasculature disease",
          "vascular disease of the skin",
          "vascular skin disease",
          "vasculature skin disease",
          "disorder of blood vessels affecting skin",
          "vascular disorder of skin",
          "vascular disorders of skin"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease that involves the superficial vasculature."
      },
      "child_count": 40,
      "reference_id": "MONDO:0019293"
    },
    {
      "id": 20682,
      "label": "benign eyelid neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4352,
        20564,
        20576
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:137911",
          "NCIT:C4354",
          "SCTID:231824001",
          "UMLS:C0339107"
        ],
        "synonyms": [
          "benign eyelid neoplasm",
          "benign eyelid tumor",
          "benign eyelid tumour",
          "benign neoplasm of eyelid",
          "benign neoplasm of the eyelid",
          "benign tumor of eyelid",
          "benign tumor of the eyelid",
          "benign tumour of eyelid",
          "benign tumour of the eyelid",
          "eyelid benign neoplasm"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A non-metastasizing neoplasm that arises from the upper or lower eyelid."
      },
      "child_count": 12,
      "reference_id": "MONDO:0021605"
    },
    {
      "id": 23107,
      "label": "neurocutaneous syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:82706",
          "MESH:D020752",
          "NANDO:2100220",
          "NCIT:C84348",
          "SCTID:78572006",
          "UMLS:C0265316"
        ],
        "synonyms": [
          "neurocutaneous syndrome",
          "Phacomatoses",
          "Phacomatosis",
          "Phakomatoses",
          "neurocutaneous disorder",
          "neurocutaneous disorders",
          "neuroectodermal dysplasia",
          "neuroectodermal dysplasia syndrome",
          "neuroectodermal dysplasia syndromes",
          "phakomatosis",
          "syndrome, neurocutaneous",
          "syndrome, neuroectodermal dysplasia",
          "syndromes, neurocutaneous",
          "syndromes, neuroectodermal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs."
      },
      "child_count": 9,
      "reference_id": "MONDO:0042983"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5091,
      "label": "skin hemangioma"
    },
    {
      "id": 16257,
      "label": "cerebrofacial arteriovenous metameric syndrome"
    },
    {
      "id": 19142,
      "label": "skin vascular disease"
    },
    {
      "id": 20682,
      "label": "benign eyelid neoplasm"
    },
    {
      "id": 23107,
      "label": "neurocutaneous syndrome"
    },
    {
      "id": 23165,
      "label": "neurovascular disorder"
    }
  ]
}