{
  "id": 18367,
  "label": "obesity due to SIM1 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018244",
  "properties": {
    "xrefs": [
      "GARD:0021580",
      "MEDGEN:1680592",
      "Orphanet:369873",
      "UMLS:C5191050"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19055,
      "label": "inherited obesity",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6875,
        12246
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018935",
          "MEDGEN:885912",
          "OMIM:601665",
          "Orphanet:77828",
          "UMLS:C4054476"
        ],
        "synonyms": [
          "genetic obesity",
          "genetic obesity (disease)",
          "leanness, inherited, autosomal recessive",
          "monogenic obesity",
          "obesity, association with, Autosomal recessive",
          "obesity, early-onset, susceptibility to, Autosomal recessive",
          "obesity, late-onset, Autosomal recessive",
          "obesity, mild, early-onset, Autosomal recessive",
          "obesity, severe, Autosomal recessive",
          "obesity, severe, and type II diabetes, Autosomal recessive",
          "obesity, susceptibility to, Autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 21,
      "reference_id": "MONDO:0019182"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19055,
      "label": "inherited obesity"
    }
  ]
}