{
  "id": 14489,
  "label": "hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013458",
  "properties": {
    "xrefs": [
      "GARD:0017569",
      "MEDGEN:462559",
      "OMIM:613845",
      "Orphanet:363694",
      "UMLS:C3151209"
    ],
    "synonyms": [
      "HUPRA syndrome",
      "hyperuricemia, pulmonary hypertension, renal failure, and alkalosis",
      "HUPRAS",
      "Hupra syndrome",
      "hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6873,
      "label": "pulmonary hypertension",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6776
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6432",
          "GARD:0027347",
          "MEDGEN:9376",
          "MESH:D006976",
          "MedDRA:10037400",
          "SCTID:70995007",
          "UMLS:C0020542",
          "icd11.foundation:1496633964"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Increased pressure within the pulmonary circulation due to lung or heart disorder."
      },
      "child_count": 6,
      "reference_id": "MONDO:0005149"
    },
    {
      "id": 16626,
      "label": "inherited renal tubular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20667,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020306",
          "MEDGEN:1826140",
          "Orphanet:183592",
          "UMLS:C5680544"
        ],
        "synonyms": [
          "genetic renal tubular disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 56,
      "reference_id": "MONDO:0015962"
    },
    {
      "id": 16918,
      "label": "mitochondrial oxidative phosphorylation disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5908
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020546",
          "MEDGEN:1825947",
          "Orphanet:223713",
          "UMLS:C5679825",
          "icd11.foundation:1204111545"
        ],
        "synonyms": [
          "OXPHOS disease",
          "OXPHOS system deficiency"
        ],
        "definition": "A multisystem disorder with variable manifestations resulting from a defect in the mitochondrial oxidative phosphorylation (OXPHOS) system."
      },
      "child_count": 48,
      "reference_id": "MONDO:0016387"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6873,
      "label": "pulmonary hypertension"
    },
    {
      "id": 16626,
      "label": "inherited renal tubular disease"
    },
    {
      "id": 16918,
      "label": "mitochondrial oxidative phosphorylation disorder"
    }
  ]
}