{
  "id": 9121,
  "label": "pseudohypoaldosteronism type 2A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007772",
  "properties": {
    "xrefs": [
      "GARD:0016775",
      "MEDGEN:327088",
      "OMIM:145260",
      "Orphanet:88938",
      "SCTID:703254001",
      "UMLS:C1840389",
      "icd11.foundation:646091849"
    ],
    "synonyms": [
      "PHA2A",
      "Gordon hyperkalemia-hypertension syndrome",
      "hyperpotassemia and hypertension, familial",
      "hypertensive hyperkalemia, familial",
      "pseudohypoaldosteronism, type IIA"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19039,
      "label": "pseudohypoaldosteronism type 2",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24056
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004553",
          "ICD9:588.89",
          "MEDGEN:259599",
          "NANDO:2200369",
          "NCIT:C123252",
          "OMIMPS:145260",
          "Orphanet:757",
          "SCTID:15689008",
          "UMLS:C1449844",
          "icd11.foundation:715347509"
        ],
        "synonyms": [
          "Gordon hyperkalemia-hypertension syndrome",
          "PHA2",
          "PHAII",
          "Spitzer-Weinstein syndrome",
          "chloride shunt syndrome",
          "familial hyperkalemic hypertension",
          "hyperkalemia-hypertension syndrome, Gordon type",
          "hypertensive hyperkalemia",
          "mineralocorticoid resistant hyperkalemia",
          "pseudohypoaldosteronism, type 2",
          "pseudohypoaldosteronism, type II",
          "Gordon syndrome",
          "hyperpotassemia and hypertension familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function."
      },
      "child_count": 5,
      "reference_id": "MONDO:0019162"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19039,
      "label": "pseudohypoaldosteronism type 2"
    }
  ]
}