{
  "id": 12989,
  "label": "mitral valve prolapse, myxomatous 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011915",
  "properties": {
    "xrefs": [
      "GARD:0015421",
      "MEDGEN:335856",
      "MESH:C564326",
      "OMIM:607829",
      "UMLS:C1843003"
    ],
    "synonyms": [
      "MMVP2",
      "mitral valve prolapse, myxomatous 2",
      "MVP2",
      "mitral valve prolapse 2",
      "myxomatous mitral valve prolapse 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9330,
      "label": "familial mitral valve prolapse",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6662,
        19556,
        23092
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003687",
          "MEDGEN:573696",
          "OMIMPS:157700",
          "Orphanet:741",
          "SCTID:233858000",
          "UMLS:C0340364"
        ],
        "synonyms": [
          "hereditary mitral valve prolapse (disease)",
          "MVP",
          "mitral valve prolapse, familial",
          "mitral valve prolapse, familial, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An instance of mitral valve prolapse (disease) that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 9,
      "reference_id": "MONDO:0008004"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9330,
      "label": "familial mitral valve prolapse"
    }
  ]
}