{
  "id": 21770,
  "label": "partial lipodystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0027767",
  "properties": {
    "xrefs": [
      "DOID:0080299",
      "GARD:0027921",
      "MEDGEN:1386287",
      "NCIT:C131296",
      "UMLS:C4316789"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Loss and redistribution of subcutaneous and/or visceral adipose tissue from specific regions of the body."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 8053,
      "label": "lipodystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6795,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:811",
          "EFO:1000727",
          "GARD:0027051",
          "HP:0009125",
          "ICD9:272.6",
          "MEDGEN:6111",
          "MESH:D008060",
          "NANDO:1200858",
          "NANDO:2100147",
          "NANDO:2200404",
          "NCIT:C97093",
          "SCTID:71325002",
          "UMLS:C0023787",
          "Wikipedia:Lipodystrophy"
        ],
        "synonyms": [
          "lipodsystrophic syndrome",
          "lipodsystrophic syndromes",
          "lipodystrophy",
          "lipodystrophy (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A congenital or acquired disorder characterized by abnormal loss or redistribution of the adipose tissue in the body."
      },
      "child_count": 10,
      "reference_id": "MONDO:0006573"
    }
  ],
  "children": [
    {
      "id": 13170,
      "label": "acquired partial lipodystrophy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19733,
        21770
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010509",
          "MEDGEN:66352",
          "MESH:C562448",
          "NANDO:1200862",
          "NCIT:C129723",
          "Orphanet:79087",
          "SCTID:75659004",
          "UMLS:C0220989",
          "icd11.foundation:2042663302"
        ],
        "synonyms": [
          "APLD",
          "Barraquer-Simons syndrome",
          "acquired partial lipodystrophy",
          "partial acquired lipodystrophy",
          "progressive cephalothoracic lipodystrophy",
          "APLD, susceptibility to",
          "lipodystophy partial progressive",
          "lipodystrophy cephalothoracic type",
          "lipodystrophy partial acquired",
          "lipodystrophy, cephalothoracic type",
          "lipodystrophy, partial, acquired, susceptibility to",
          "lipodystrophy, partial, progressive",
          "susceptibility to partial acquired lipodystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A lipodystrophy characterized by the association of lipoatrophy of the upper part of the body and lipohypertrophy of the thighs."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012104"
    },
    {
      "id": 19732,
      "label": "familial partial lipodystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19731,
        20345,
        21770
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050440",
          "GARD:0011962",
          "MEDGEN:124408",
          "MESH:D052496",
          "NANDO:1200861",
          "NCIT:C84708",
          "NORD:1131",
          "OMIMPS:151660",
          "Orphanet:98306",
          "SCTID:49292002",
          "UMLS:C0271694",
          "icd11.foundation:1661968243"
        ],
        "synonyms": [
          "FPLD",
          "congenital partial lipodystrophy",
          "genetic partial lipodystrophy",
          "lipodystrophy, familial partial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Familial partial lipodystrophy (FPLD) is a group of rare genetic lipodystrophic syndromes characterized, in most cases, by fat loss from the limbs and buttocks, from childhood or early adulthood, and often associated with acanthosis nigricans, insulin resistance, diabetes, hypertriglyceridemia and liver steatosis."
      },
      "child_count": 30,
      "reference_id": "MONDO:0020088"
    }
  ],
  "roots": [
    {
      "id": 8053,
      "label": "lipodystrophy"
    }
  ]
}