{
  "id": 10306,
  "label": "cutis marmorata telangiectatica congenita",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009055",
  "properties": {
    "xrefs": [
      "GARD:0006228",
      "HP:0025107",
      "ICD9:757.8",
      "MEDGEN:83381",
      "MESH:C536226",
      "OMIM:219250",
      "Orphanet:1556",
      "SCTID:254778000",
      "UMLS:C0345419",
      "icd11.foundation:1359154853"
    ],
    "synonyms": [
      "CMTC",
      "cutis marmorata telangiectatica congenita",
      "cutis marmorata telangiectatica congenita (disease)",
      "Van Lohuizen syndrome",
      "hereditary cutis marmorata telangiectatica congenita"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Cutis marmorata telangiectatica congenita (CMTC) is a congenital localized or generalized vascular anomaly characterized by a persistent cutis marmorata pattern with a marbled bluish to deep purple appearance, spider nevus-like telangiectasia, phlebectasia and, occasionally, ulceration and atrophy of the affected skin."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16809,
      "label": "capillary malformation"
    },
    {
      "id": 19142,
      "label": "skin vascular disease"
    }
  ]
}