{
  "id": 13087,
  "label": "capillary malformation-arteriovenous malformation syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012016",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "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"
    },
    {
      "id": 16809,
      "label": "capillary malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:90955",
          "Orphanet:211247",
          "SCTID:234118009",
          "UMLS:C0340803"
        ],
        "synonyms": [
          "congenital malformation of capillary",
          "rare capillary malformation"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0016231"
    }
  ],
  "children": [
    {
      "id": 20184,
      "label": "capillary malformation-arteriovenous malformation 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        13087
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009787",
          "ICD9:759.6",
          "MEDGEN:1648501",
          "OMIM:608354",
          "OMIM:608355",
          "Orphanet:693907",
          "SCTID:234143003",
          "UMLS:C4747394"
        ],
        "synonyms": [
          "CMAVM1",
          "RASA1-related capillary malformation-arteriovenous malformation",
          "capillary malformation-arteriovenous malformation 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020783"
    },
    {
      "id": 20185,
      "label": "capillary malformation-arteriovenous malformation 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        13087,
        24476
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020785"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 16809,
      "label": "capillary malformation"
    }
  ]
}