{
  "id": 9412,
  "label": "familial multiple nevi flammei",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008094",
  "properties": {
    "xrefs": [
      "DOID:0111529",
      "GARD:0003986",
      "MEDGEN:419699",
      "MedDRA:10067193",
      "NCIT:C3840",
      "OMIM:163000",
      "Orphanet:624",
      "SCTID:416377005",
      "UMLS:C2931029"
    ],
    "synonyms": [
      "Nevus flammeus",
      "Salmon patch Nevus",
      "capillary malformations, congenital, 1, somatic, mosaic",
      "familial multiple port-wine stains",
      "port wine Nevus",
      "port wine birthmark",
      "port wine stain",
      "port wine stain of skin",
      "port wine stain of the skin",
      "port wine type hemangioma",
      "port-wine stain of skin",
      "CMC",
      "capillary malformations",
      "capillary malformations, congenital",
      "nevi flammei, familial multiple",
      "port-wine stain",
      "port-wine stain familial multiple"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A congenital vascular malformation in the skin (birthmark) characterized by the presence of dilated capillaries. The affected area of the skin is flat and reddish-purplish in color."
  },
  "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"
    },
    {
      "id": 20710,
      "label": "vascular ectasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:8080",
          "NCIT:C45481",
          "UMLS:C0002959"
        ],
        "synonyms": [
          "vascular ectasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0021658"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16809,
      "label": "capillary malformation"
    },
    {
      "id": 19142,
      "label": "skin vascular disease"
    },
    {
      "id": 20710,
      "label": "vascular ectasia"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}