{
  "id": 26043,
  "label": "cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome due to TAB2 mutation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0971094",
  "properties": {
    "xrefs": [
      "GARD:0027175",
      "MEDGEN:1863549",
      "Orphanet:664401",
      "UMLS:C5925073"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16971,
      "label": "polyvalvular heart disease syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6967,
        16088
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020594",
          "MEDGEN:1376905",
          "Orphanet:228410",
          "SCTID:723448007",
          "UMLS:C4509918"
        ],
        "synonyms": [
          "PHD syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Polyvalvular heart disease syndrome is a recently described syndrome characterized by the combination of polyvalvular heart disease, short stature, facial anomalies and intellectual deficit."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016460"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16971,
      "label": "polyvalvular heart disease syndrome"
    }
  ]
}