{
  "id": 25460,
  "label": "hypomagnesemia 7, renal, with or without dilated cardiomyopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859328",
  "properties": {
    "xrefs": [
      "DOID:0060972",
      "GARD:0026701",
      "MEDGEN:1824039",
      "OMIM:620152",
      "UMLS:C5774266"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18259,
      "label": "familial primary hypomagnesemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6470,
        16626,
        17990
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060879",
          "GARD:0025126",
          "MEDGEN:57481",
          "NCIT:C123263",
          "OMIMPS:602014",
          "Orphanet:34526",
          "SCTID:80710001",
          "UMLS:C0151723"
        ],
        "synonyms": [
          "hypomagnesemia",
          "familial primary hypomagnesemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration."
      },
      "child_count": 15,
      "reference_id": "MONDO:0018100"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18259,
      "label": "familial primary hypomagnesemia"
    }
  ]
}