{
  "id": 20185,
  "label": "capillary malformation-arteriovenous malformation 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020785",
  "properties": {
    "xrefs": [
      "GARD:0016307",
      "MEDGEN:1648502",
      "OMIM:618196",
      "Orphanet:693912",
      "UMLS:C4748670"
    ],
    "synonyms": [
      "CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2",
      "CMAVM2"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 13087,
      "label": "capillary malformation-arteriovenous malformation syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16809
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0011904",
          "ICD9:747.69",
          "MEDGEN:334007",
          "MESH:C564254",
          "NCIT:C179668",
          "OMIMPS:608354",
          "Orphanet:137667",
          "SCTID:703533007",
          "UMLS:C1842180"
        ],
        "synonyms": [
          "CM-AVM",
          "CM-AVM syndrome",
          "CMAVM",
          "capillary malformation without arteriovenous malformation",
          "capillary malformation-arteriovenous malformation"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "This syndrome is characterized by the association of multiple capillary malformations (CM) with an arteriovenous malformation (AVM) and arteriovenous fistulas."
      },
      "child_count": 4,
      "reference_id": "MONDO:0012016"
    },
    {
      "id": 24476,
      "label": "EPHB4-associated vascular malformation spectrum",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        21326
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any vascular malformation in which the cause of the disease is a variation in the EPHB4 gene."
      },
      "child_count": 4,
      "reference_id": "MONDO:0700080"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 13087,
      "label": "capillary malformation-arteriovenous malformation syndrome"
    },
    {
      "id": 24476,
      "label": "EPHB4-associated vascular malformation spectrum"
    }
  ]
}