{
  "id": 13265,
  "label": "familial pseudohyperkalemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012204",
  "properties": {
    "xrefs": [
      "GARD:0016785",
      "MEDGEN:324588",
      "MESH:C563785",
      "OMIM:609153",
      "Orphanet:90044",
      "SCTID:717254007",
      "UMLS:C1836705",
      "icd11.foundation:1653996588"
    ],
    "synonyms": [
      "PSHK2",
      "pseudohyperkalemia, familial, 2, due to red cell leak",
      "cryohydrocytosis, mild",
      "pseudohyperkalemia Chiswick",
      "pseudohyperkalemia East London",
      "pseudohyperkalemia Falkirk",
      "pseudohyperkalemia Lille"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "An inherited, mild, non-hemolytic subtype of hereditary stomatocytosis that is associated with a temperature-dependent anomaly in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C. FP is not associated with additional hematological abnormalities, although affected individuals may show some mild abnormalities like macrocytosis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5573,
      "label": "familial hemolytic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5550,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:589",
          "GARD:0006167",
          "ICD9:282",
          "ICD9:282.9",
          "MEDGEN:1919",
          "MESH:D000745",
          "NANDO:2100183",
          "NCIT:C34379",
          "SCTID:42601008",
          "UMLS:C0002881"
        ],
        "synonyms": [
          "congenital hemolytic anemia",
          "hereditary hemolytic anemia",
          "anaemia hemolytic congenital",
          "anemia hemolytic congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies."
      },
      "child_count": 46,
      "reference_id": "MONDO:0003689"
    },
    {
      "id": 19735,
      "label": "hereditary stomatocytosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5550
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019456",
          "ICD9:282.8",
          "MEDGEN:490161",
          "NANDO:2200623",
          "Orphanet:98365",
          "SCTID:14087004",
          "UMLS:C1262483",
          "icd11.foundation:2067120097"
        ],
        "synonyms": [
          "hereditary stomatocytic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0020102"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5573,
      "label": "familial hemolytic anemia"
    },
    {
      "id": 19735,
      "label": "hereditary stomatocytosis"
    }
  ]
}