{
  "id": 13890,
  "label": "hypophosphatemic nephrolithiasis/osteoporosis 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012850",
  "properties": {
    "xrefs": [
      "DOID:0080077",
      "GARD:0018346",
      "MEDGEN:436776",
      "MESH:C567363",
      "OMIM:612286",
      "UMLS:C2676786"
    ],
    "synonyms": [
      "hypophosphatemic nephrolithiasis/osteoporosis type 1",
      "nephrolithiasis/osteoporosis, hypophosphatemic, type 1",
      "NPHLOP1",
      "nephrolithiasis/osteoporosis, hypophosphatemic, 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2718,
      "label": "nephrolithiasis/osteoporosis, hypophosphatemic",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6992
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080655",
          "GARD:0022708",
          "OMIMPS:612286"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0000079"
    },
    {
      "id": 3571,
      "label": "impaired renal function disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6948
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11705",
          "ICD10CM:N25",
          "ICD9:588.8",
          "ICD9:588.89",
          "ICD9:588.9",
          "MEDGEN:574572",
          "SCTID:197663003",
          "UMLS:C0341677"
        ],
        "synonyms": [
          "disease of kidney",
          "kidney disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Any disease in which the causes of the disease is a perturbation of the kidney leading to its dysfunction."
      },
      "child_count": 4,
      "reference_id": "MONDO:0001343"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6948
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "genetic renal disease",
          "inherited kidney disease",
          "inherited renal disorder",
          "nephrogenetic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system."
      },
      "child_count": 52,
      "reference_id": "MONDO:0100191"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2718,
      "label": "nephrolithiasis/osteoporosis, hypophosphatemic"
    },
    {
      "id": 3571,
      "label": "impaired renal function disease"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder"
    }
  ]
}