{
  "id": 9100,
  "label": "hypercholesterolemia, familial, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007750",
  "properties": {
    "xrefs": [
      "GARD:0024574",
      "MEDGEN:152875",
      "NANDO:2200602",
      "OMIM:143890",
      "SCTID:398036000",
      "UMLS:C0745103"
    ],
    "synonyms": [
      "FHCL1",
      "LDL cholesterol level QTL2",
      "LDL receptor disorder",
      "hypercholesterolemia, familial",
      "hypercholesterolemia, familial, 1",
      "hypercholesterolemia, familial, due to ldlr defect, modifier of",
      "hypercholesterolemia, familial, modifier of",
      "hypercholesterolemic xanthomatosis, familial",
      "hyperlipoproteinemia, type 2",
      "hyperlipoproteinemia, type 2A",
      "FHC",
      "hyper-low-density-lipoproteinemia",
      "hypercholesterolemia, susceptibility to",
      "low density lipoprotein cholesterol level quantitative trait locus 2"
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7106,
      "label": "familial hypercholesterolemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3564,
        22978
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13810",
          "EFO:0004911",
          "ICD10CM:E78.01",
          "ICD9:V19.8",
          "MEDGEN:5688",
          "NANDO:2200602",
          "NCIT:C34704",
          "OMIMPS:143890",
          "SCTID:190773008",
          "UMLS:C0020445"
        ],
        "synonyms": [
          "hyperlipoproteinemia type II",
          "type II hyperlipidemia"
        ],
        "definition": "An inheritable form of hyperlipidemia, in which there are excess lipids in the blood."
      },
      "child_count": 10,
      "reference_id": "MONDO:0005439"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7106,
      "label": "familial hypercholesterolemia"
    }
  ]
}