{
  "id": 16288,
  "label": "autosomal dominant coarctation of aorta",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015445",
  "properties": {
    "xrefs": [
      "GARD:0018722",
      "MEDGEN:443900",
      "Orphanet:1455",
      "UMLS:C2930803"
    ],
    "synonyms": [
      "aorta coarctation, autosomal dominant",
      "autosomal dominant aorta coarctation"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Autosomal dominant form of aorta coarctation."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 8740,
      "label": "aorta coarctation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7210,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0051054",
          "EFO:1001267",
          "GARD:0005828",
          "ICD10CM:Q25.1",
          "ICD9:747.10",
          "MEDGEN:1617",
          "MESH:D001017",
          "MedDRA:10009807",
          "NANDO:2200283",
          "NANDO:2200284",
          "NCIT:C84567",
          "OMIM:120000",
          "Orphanet:1457",
          "SCTID:7305005",
          "UMLS:C0003492",
          "icd11.foundation:1524185114"
        ],
        "synonyms": [
          "aortic coarctation",
          "coarctation of aorta",
          "coarctation of the aorta"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Congenital narrowing of a segment of the aorta. Signs and symptoms include hypertension, muscle weakness, shortness of breath, headaches and leg cramps."
      },
      "child_count": 6,
      "reference_id": "MONDO:0007345"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 8740,
      "label": "aorta coarctation"
    }
  ]
}