{
  "id": 13740,
  "label": "renal tubular acidosis, distal, 4, with hemolytic anemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012700",
  "properties": {
    "xrefs": [
      "GARD:0012354",
      "MEDGEN:1771439",
      "OMIM:611590",
      "Orphanet:93610",
      "UMLS:C5436235"
    ],
    "synonyms": [
      "dRTA with anaemia",
      "dRTA with anemia",
      "distal renal tubular acidosis 4 with hemolytic anaemia",
      "distal renal tubular acidosis 4 with hemolytic anemia",
      "distal renal tubular acidosis with anaemia",
      "distal renal tubular acidosis with anemia",
      "RTA, distal, autosomal recessive, with hemolytic Anaemia",
      "renal tubular acidosis, distal, with hemolytic anaemia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "A very rare form of distal renal tubular acidosis (dRTA) characterized by a defect in renal acidification and hereditary hemolytic anemia."
  },
  "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": 18488,
      "label": "autosomal recessive distal renal tubular acidosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        29329
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004666",
          "MEDGEN:351142",
          "Orphanet:402041",
          "UMLS:C1864498"
        ],
        "synonyms": [
          "AR dRTA",
          "autosomal recessive distal RTA",
          "autosomal recessive distal renal tubular acidosis (disease)",
          "distal renal tubular acidosis (disease), autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "The autosomal recessive form of distal renal tubular acidosis (dRTA) characterized by hypokalemic hyperchloremic metabolic acidosis. Deafness often occurs either early or later on in life but may be absent or never be diagnosed."
      },
      "child_count": 6,
      "reference_id": "MONDO:0018440"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5573,
      "label": "familial hemolytic anemia"
    },
    {
      "id": 18488,
      "label": "autosomal recessive distal renal tubular acidosis"
    }
  ]
}