{
  "id": 25295,
  "label": "BDV syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859150",
  "properties": {
    "xrefs": [
      "GARD:0027308",
      "MEDGEN:1785671",
      "OMIM:619326",
      "Orphanet:633028",
      "UMLS:C5543403"
    ],
    "synonyms": [
      "CPE-related Prader-Willi-like syndrome"
    ],
    "categories": [
      {
        "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": 18437,
      "label": "Prader-Willi-like syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        16088,
        16526,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021641",
          "MEDGEN:816207",
          "Orphanet:398073",
          "UMLS:C3809877"
        ],
        "synonyms": [
          "PWS-like"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Prader-Willi-like syndrome is a rare, genetic, endocrine disease characterized by manifestations of a Prader-Willi syndrome phenotype (including obesity, hyperphagia, hypotonia, psychomotor delay, intellectual disability, small hands/feet, hypogonadism, growth hormone deficiency and characteristic facial features) occurring in the absence of 15q11-q13 genomic abnormalities."
      },
      "child_count": 12,
      "reference_id": "MONDO:0018354"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18437,
      "label": "Prader-Willi-like syndrome"
    }
  ]
}