{
  "id": 18821,
  "label": "Cobb syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018893",
  "properties": {
    "xrefs": [
      "GARD:0011892",
      "ICD9:239.2",
      "MEDGEN:91079",
      "MedDRA:10068841",
      "NCIT:C4485",
      "Orphanet:53721",
      "SCTID:254774003",
      "UMLS:C0346068",
      "icd11.foundation:1451924695"
    ],
    "synonyms": [
      "Cobb's syndrome",
      "SAMS 1-31",
      "cutaneomeningospinal angiomatosis",
      "spinal arteriovenous metameric syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Cobb syndrome is defined by the association of vascular cutaneous (venous or arteriovenous), muscular (arteriovenous), osseous (arteriovenous) and medullary (arteriovenous) lesions at the same metamere or spinal segment. This segmental distribution may involve one or many of the 31 metameres present in humans. Only 16% of the medullary lesions are multiple and have a clearly metameric distribution."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3493,
      "label": "arteriovenous hemangioma/malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7994
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "CSP:0571-2717",
          "DOID:11294",
          "HP:0100026",
          "ICDO:9123/0",
          "MEDGEN:137780",
          "MESH:D001165",
          "NCIT:C2882",
          "SCTID:233982006",
          "UMLS:C0334533"
        ],
        "synonyms": [
          "arteriovenous angioma",
          "arteriovenous hemangioma",
          "arteriovenous hemangioma/malformation",
          "racemose aneurysm (morphologic abnormality)",
          "racemose hemangioma (morphologic abnormality)",
          "arteriovenous malformation",
          "cirsoid aneurysm"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A benign vascular lesion characterized by the presence of a complex network of communicating arterial and venous vascular structures."
      },
      "child_count": 7,
      "reference_id": "MONDO:0001256"
    },
    {
      "id": 5091,
      "label": "skin hemangioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7994,
        20564
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:471",
          "MEDGEN:151951",
          "NCIT:C4905",
          "SCTID:93471006",
          "UMLS:C0687140"
        ],
        "synonyms": [
          "angioma of skin",
          "angioma of the skin",
          "hemangioma of skin",
          "hemangioma of the skin",
          "hemangioma of zone of skin",
          "skin angioma",
          "skin hemangioma",
          "zone of skin hemangioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A hemangioma arising from the skin."
      },
      "child_count": 20,
      "reference_id": "MONDO:0003110"
    },
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        20011,
        20301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019921",
          "MEDGEN:14326",
          "MESH:D009386",
          "NCIT:C3266",
          "Orphanet:140162",
          "SCTID:699346009",
          "UMLS:C0027672"
        ],
        "synonyms": [
          "cancer syndrome, hereditary",
          "cancer syndromes, hereditary",
          "familial neoplastic syndrome",
          "familial tumor syndrome",
          "familial tumour syndrome",
          "hereditary cancer syndrome",
          "hereditary cancer syndromes",
          "hereditary neoplastic syndrome",
          "hereditary neoplastic syndromes",
          "hereditary tumor syndrome",
          "hereditary tumour syndrome",
          "inherited cancer syndrome",
          "inherited cancer-predisposing syndrome",
          "neoplastic syndrome, hereditary",
          "syndrome, hereditary cancer",
          "syndrome, hereditary neoplastic",
          "syndromes, hereditary cancer",
          "syndromes, hereditary neoplastic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "The inherited predisposition toward getting a tumor."
      },
      "child_count": 351,
      "reference_id": "MONDO:0015356"
    },
    {
      "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": 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": 3493,
      "label": "arteriovenous hemangioma/malformation"
    },
    {
      "id": 5091,
      "label": "skin hemangioma"
    },
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome"
    },
    {
      "id": 19142,
      "label": "skin vascular disease"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}