{
  "id": 25803,
  "label": "lipodystrophy, congenital generalized, type 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958023",
  "properties": {
    "xrefs": [
      "GARD:0026914",
      "MEDGEN:1847991",
      "OMIM:620680",
      "UMLS:C5882745"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8021,
      "label": "congenital generalized lipodystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19731,
        21769
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050585",
          "EFO:1000681",
          "GARD:0024436",
          "HP:0009059",
          "MEDGEN:67438",
          "NANDO:1200859",
          "NORD:998",
          "OMIMPS:608594",
          "SCTID:284449005",
          "UMLS:C0221032"
        ],
        "synonyms": [
          "congenital generalised lipodystrophy (disease)",
          "congenital generalized lipodystrophy",
          "congenital generalized lipodystrophy (disease)",
          "familial generalised lipodystrophy",
          "familial generalized lipodystrophy",
          "hereditary generalised lipodystrophy",
          "hereditary generalized lipodystrophy",
          "lipodystrophy, congenital generalised",
          "lipodystrophy, congenital generalized"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An extremely rare autosomal recessive condition, characterized by an extreme scarcity of fat in the subcutaneous tissues."
      },
      "child_count": 10,
      "reference_id": "MONDO:0006536"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8021,
      "label": "congenital generalized lipodystrophy"
    }
  ]
}