{
  "id": 10078,
  "label": "familial apolipoprotein C-II deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008810",
  "properties": {
    "xrefs": [
      "DOID:0111418",
      "GARD:0000759",
      "MEDGEN:328375",
      "OMIM:207750",
      "Orphanet:309020",
      "SCTID:33513003",
      "UMLS:C1720779",
      "icd11.foundation:877401371"
    ],
    "synonyms": [
      "familial apoC-II deficiency",
      "familial apolipoprotein C-II deficiency",
      "hyperlipoproteinemia, type IB",
      "Apoc2 deficiency",
      "C-II Anapolipoproteinemia",
      "apolipoprotein C-II deficiency",
      "hyperlipoproteinemia, type 1B"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3564,
      "label": "familial hyperlipidemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4594,
        20414
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1168",
          "GARD:0022924",
          "MEDGEN:675194",
          "NANDO:2200603",
          "UMLS:C0700623"
        ],
        "synonyms": [
          "hyperlipemia",
          "hyperlipidaemia",
          "hereditary hyperlipidemia (disease)",
          "familial hyperlipemia",
          "familial hyperlipoproteinemia"
        ],
        "definition": "An instance of hyperlipidemia (disease) that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 20,
      "reference_id": "MONDO:0001336"
    },
    {
      "id": 16607,
      "label": "syndromic dyslipidemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        4594
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020232",
          "MEDGEN:1826171",
          "Orphanet:181437",
          "SCTID:109041000119107",
          "UMLS:C5680608"
        ],
        "synonyms": [
          "complex dyslipidaemia",
          "complex dyslipidemia",
          "syndrome associated with inherited lipid metabolism disorder",
          "syndromic inherited lipid metabolism disorder",
          "rare syndromic dyslipidaemia",
          "rare syndromic dyslipidemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A inherited lipid metabolism disorder that is part of a larger syndrome."
      },
      "child_count": 58,
      "reference_id": "MONDO:0015905"
    },
    {
      "id": 18634,
      "label": "familial chylomicronemia syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111417",
          "GARD:0006414",
          "MEDGEN:1778100",
          "Orphanet:444490",
          "UMLS:C5442313"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A rare autosomal recessive disease characterized by the buildup in the blood of fat particles called chylomicrons (chylomicronemia), severe hypertriglyceridemia, and the risk of recurrent and potentially fatal pancreatitis and other complications. It is caused by mutations in the gene encoding LPL or, less frequently, by mutations in genes encoding other proteins necessary for LPL function."
      },
      "child_count": 5,
      "reference_id": "MONDO:0018637"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3564,
      "label": "familial hyperlipidemia"
    },
    {
      "id": 16607,
      "label": "syndromic dyslipidemia"
    },
    {
      "id": 18634,
      "label": "familial chylomicronemia syndrome"
    }
  ]
}