{
  "id": 16809,
  "label": "capillary malformation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016231",
  "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"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 6,
  "parents": [
    {
      "id": 7065,
      "label": "vascular disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6736
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:178",
          "EFO:0004264",
          "ICD10CM:I00-I99",
          "ICD10CM:I70-I79",
          "ICD9:442.9",
          "MEDGEN:22621",
          "MESH:D014652",
          "NANDO:2100294",
          "NCIT:C35117",
          "SCTID:27550009",
          "UMLS:C0042373"
        ],
        "synonyms": [
          "disease of vasculature",
          "disease or disorder of vasculature",
          "disorder of vasculature",
          "vascular disorder",
          "vasculature disease",
          "vasculature disease or disorder",
          "vasculopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A general term used to describe any disease affecting blood vessels]. It includes vascular abnormalities caused by degenerative, metabolic and inflammatory conditions, embolic diseases, coagulative disorders, and functional disorders such as posteri or reversible encephalopathy syndrome."
      },
      "child_count": 60,
      "reference_id": "MONDO:0005385"
    }
  ],
  "children": [
    {
      "id": 5541,
      "label": "stork bite",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16809
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5806",
          "MEDGEN:870384",
          "SCTID:254211001",
          "UMLS:C4024829",
          "icd11.foundation:400551861"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0003653"
    },
    {
      "id": 9412,
      "label": "familial multiple nevi flammei",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16809,
        19142,
        20710,
        23867
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008094"
    },
    {
      "id": 10306,
      "label": "cutis marmorata telangiectatica congenita",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16809,
        19142
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009055"
    },
    {
      "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": 19053,
      "label": "hereditary hemorrhagic telangiectasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        3779,
        16809,
        19507
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1270",
          "GARD:0006626",
          "ICD10CM:I78.0",
          "ICD9:448.0",
          "MEDGEN:52657",
          "MESH:D013683",
          "MedDRA:10019883",
          "NANDO:1200744",
          "NANDO:2100296",
          "NANDO:2201034",
          "NCIT:C35064",
          "NORD:1229",
          "OMIMPS:187300",
          "Orphanet:774",
          "SCTID:21877004",
          "UMLS:C0039445",
          "icd11.foundation:714406192"
        ],
        "synonyms": [
          "HHT",
          "Osler-Weber-Rendu disease",
          "Rendu-Osler disease",
          "Rendu-Osler-Weber disease",
          "hereditary hemorrhagic telangiectasia",
          "telangiectasia, hereditary Hemorrahagic, of Rendu, Osler",
          "telangiectasia, hereditary hemorrhagic"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal hemorrhagic telangiectasias and visceral shunting."
      },
      "child_count": 20,
      "reference_id": "MONDO:0019180"
    },
    {
      "id": 19544,
      "label": "angioma serpiginosum",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4409,
        5091,
        16809,
        19142
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4028",
          "GARD:0015021",
          "MEDGEN:75528",
          "NCIT:C3926",
          "Orphanet:95429",
          "SCTID:49465005",
          "UMLS:C0263637",
          "icd11.foundation:1724787481"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Angioma serpiginosum (AS) is a benign congenital skin disease characterized by progressive dilation of the subepidermal skin vessels manifesting as purple punctate lesions usually appearing on the lower limbs and buttocks and following the lines of Blaschko."
      },
      "child_count": 8,
      "reference_id": "MONDO:0019803"
    }
  ],
  "roots": [
    {
      "id": 7065,
      "label": "vascular disorder"
    }
  ]
}