{
  "id": 8215,
  "label": "fibromuscular dysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006761",
  "properties": {
    "xrefs": [
      "EFO:1000938",
      "GARD:0027765",
      "MEDGEN:4700",
      "MESH:C537929",
      "MESH:D005352",
      "MedDRA:10054794",
      "NCIT:C84714",
      "OMIM:135580",
      "Orphanet:336",
      "Orphanet:698012",
      "UMLS:C0016052",
      "icd11.foundation:280853107"
    ],
    "synonyms": [
      "FMDA",
      "fibromuscular dysplasia",
      "fibromuscular dysplasia of arteries"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A disorder characterized by fibrous thickening of the arterial wall resulting in narrowing of the arterial lumen. It most often affects the renal artery and less often the carotid artery and abdominal arteries. It can cause hypertension and aneurysm formation."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 2933,
      "label": "arterial disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050828",
          "ICD9:447.8",
          "ICD9:447.9",
          "MEDGEN:208875",
          "NCIT:C35317",
          "SCTID:359557001",
          "UMLS:C0852949"
        ],
        "synonyms": [
          "arterial disease",
          "arterial disorder",
          "arteriopathy",
          "artery disease",
          "artery disease or disorder",
          "disease of artery",
          "disease or disorder of artery",
          "disorder of artery"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An impairment of the structure or function of the blood vessels which carry blood away from the heart."
      },
      "child_count": 30,
      "reference_id": "MONDO:0000473"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    }
  ],
  "children": [
    {
      "id": 26410,
      "label": "fibromuscular dysplasia of the cervical and intracranial arteries",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8215
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:698036"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0980997"
    },
    {
      "id": 26411,
      "label": "fibromuscular dysplasia of the renal arteries",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7210,
        8215
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:698043"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0980998"
    },
    {
      "id": 26412,
      "label": "fibromuscular dysplasia of the coronary arteries",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6748,
        8215,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:698059"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0980999"
    },
    {
      "id": 26413,
      "label": "fibromuscular dysplasia of the visceral arteries",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8215
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:698063"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0981000"
    },
    {
      "id": 26414,
      "label": "fibromuscular dysplasia of the arteries of the extremities",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8215
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:698069"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0981001"
    }
  ],
  "roots": [
    {
      "id": 2933,
      "label": "arterial disorder"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}