{
  "id": 19496,
  "label": "atypical hemolytic-uremic syndrome with H factor anomaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019738",
  "properties": {
    "xrefs": [
      "Orphanet:93579"
    ],
    "synonyms": [
      "D-HUS with H factor anomaly",
      "aHUS with H factor anomaly",
      "atypical HUS with H factor anomaly",
      "hemolytic-uremic syndrome without diarrhea with H factor anomaly",
      "hemolytic-uremic syndrome without diarrhoea with H factor anomaly"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10567,
      "label": "hemolytic uremic syndrome, atypical, susceptibility to, 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20011
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:412743",
          "OMIM:235400",
          "UMLS:C2749604"
        ],
        "synonyms": [
          "hemolytic uremic syndrome, atypical, susceptibility to",
          "hemolytic uremic syndrome, atypical, susceptibility to, 1",
          "hemolytic uremic syndrome, atypical, susceptibility to, type 1",
          "AHUS1",
          "Ahus, susceptibility to, 1",
          "hemolytic uremic syndrome, typical",
          "susceptibility to atypical hemolytic uremic syndrome 1"
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0009335"
    },
    {
      "id": 16818,
      "label": "atypical hemolytic-uremic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5701,
        19495,
        25595
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080301",
          "GARD:0008702",
          "MEDGEN:444141",
          "MESH:D065766",
          "NANDO:1200473",
          "NANDO:1200474",
          "NANDO:2200131",
          "NANDO:2200641",
          "NCIT:C123223",
          "NORD:822",
          "Orphanet:2134",
          "UMLS:C2931788"
        ],
        "synonyms": [
          "Atypical Hemolytic Uremic Syndrome",
          "D-HUS",
          "aHUS",
          "atypical HUS",
          "atypical hemolytic uremic syndrome",
          "hemolytic-uremic syndrome without diarrhea",
          "hemolytic-uremic syndrome without diarrhoea",
          "non-diarrhea-associated hemolytic uremic syndrome",
          "D-minus hemolytic uremic syndrome (D-HUS)",
          "HUS, atypical"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A rare, genetic thrombotic microangiopathy due to dysregulation of the alternative complement pathway and characterized by the triad of hemolytic anemia, thrombocytopenia, and acute renal dysfunction."
      },
      "child_count": 16,
      "reference_id": "MONDO:0016244"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10567,
      "label": "hemolytic uremic syndrome, atypical, susceptibility to, 1"
    },
    {
      "id": 16818,
      "label": "atypical hemolytic-uremic syndrome"
    }
  ]
}