{
  "id": 8906,
  "label": "autosomal dominant Ehlers-Danlos syndrome, vascular type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007524",
  "properties": {
    "xrefs": [
      "DOID:14756",
      "GARD:0024560",
      "MEDGEN:541286",
      "OMIM:130050",
      "UMLS:C0268339"
    ],
    "synonyms": [
      "EDS 4",
      "Ehlers-Danlos syndrome, vascular type",
      "Ehlers-Danlos syndrome, type IV, autosomal dominant",
      "Ehlers-Danlos syndrome, vascular type, autosomal dominant",
      "autosomal dominant Ehlers-Danlos syndrome, vascular type",
      "EDSVASC",
      "Ehlers-Danlos syndrome, Ecchymotic type",
      "Ehlers-Danlos syndrome, arterial type",
      "Ehlers-Danlos syndrome, sack-Barabas type",
      "autosomal dominant type IV Ehlers-Danlos syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "The autosomal dominant form of the vascular type of Ehlers-Danlos syndrome. vEDS is almost always inherited in an autosomal dominant manner but rare examples of biallelic inheritance have been reported."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 17633,
      "label": "Ehlers-Danlos syndrome, vascular type",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7065,
        19720
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002082",
          "MEDGEN:82790",
          "NANDO:1200648",
          "NANDO:2201258",
          "NCIT:C125699",
          "Orphanet:286",
          "SCTID:17025000",
          "UMLS:C0268338",
          "icd11.foundation:1202686415"
        ],
        "synonyms": [
          "EDS IV",
          "EDS type 4",
          "Ehlers-Danlos syndrome type 4",
          "Ehlers-Danlos syndrome type IV",
          "Ehlers-Danlos syndrome, type IV",
          "Ehlers-Danlos syndrome, vascular type",
          "sack-Barabas syndrome",
          "EDS IV (formerly)",
          "EDS type 4 (formerly)",
          "EDS4 (formerly)",
          "Ehlers Danlos syndrome, arterial type",
          "Ehlers Danlos syndrome, ecchymotic type",
          "Ehlers Danlos syndrome, sack-Barabas type",
          "Ehlers-Danlos syndrome type 4 (formerly)",
          "Ehlers-Danlos syndrome type IV (formerly)",
          "vEDS",
          "vascular EDS",
          "vascular Ehlers-Danlos syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS."
      },
      "child_count": 4,
      "reference_id": "MONDO:0017314"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 17633,
      "label": "Ehlers-Danlos syndrome, vascular type"
    }
  ]
}