{
  "id": 16537,
  "label": "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015783",
  "properties": {
    "xrefs": [
      "DECIPHER:14",
      "GARD:0020138",
      "MEDGEN:1826083",
      "Orphanet:177901",
      "UMLS:C5680507"
    ],
    "synonyms": [
      "Prader-Willi syndrome (Type 1)"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19782,
      "label": "Prader-Willi syndrome due to paternal 15q11q13 deletion",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        9606,
        17332
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019576",
          "MEDGEN:1826129",
          "Orphanet:98793",
          "UMLS:C5681699"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0020301"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19782,
      "label": "Prader-Willi syndrome due to paternal 15q11q13 deletion"
    }
  ]
}