{
  "id": 10570,
  "label": "hepatic veno-occlusive disease-immunodeficiency syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009338",
  "properties": {
    "xrefs": [
      "DOID:0112254",
      "GARD:0010083",
      "MEDGEN:344659",
      "MESH:C537257",
      "NANDO:1200341",
      "NANDO:2200714",
      "OMIM:235550",
      "Orphanet:79124",
      "SCTID:724361001",
      "UMLS:C1856128",
      "icd11.foundation:712514250"
    ],
    "synonyms": [
      "VODI syndrome",
      "VODI",
      "familial veno-occlusive disease with immunodeficiency",
      "hepatic veno-occlusive disease with immunodeficiency",
      "hepatic venoocclusive disease with immunodeficiency",
      "veno-occlusive disease and immunodeficiency syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Hepatic veno-occlusive disease-immunodeficiency syndrome is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5658,
      "label": "inborn error of immunity",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:612",
          "GARD:0019813",
          "MEDGEN:585013",
          "MESH:D007153",
          "NANDO:1200320",
          "NANDO:2100204",
          "Orphanet:101997",
          "SCTID:58606001",
          "UMLS:C0398686"
        ],
        "synonyms": [
          "IEI",
          "inborn errors of immunity",
          "primary immunodeficiency disease",
          "antibody deficiency syndrome",
          "antibody deficiency syndromes",
          "deficiency syndrome, antibody",
          "deficiency syndrome, immunologic",
          "deficiency syndrome, immunological",
          "deficiency syndromes, antibody",
          "deficiency syndromes, immunologic",
          "deficiency syndromes, immunological",
          "immune deficiency disorder",
          "immunodeficiency syndrome",
          "immunologic deficiency syndrome",
          "immunological deficiency syndrome",
          "immunological deficiency syndromes",
          "primary immunodeficiency",
          "syndrome, antibody deficiency",
          "syndrome, immunologic deficiency",
          "syndrome, immunological deficiency",
          "syndromes, antibody deficiency",
          "syndromes, immunologic deficiency",
          "syndromes, immunological deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder in which the immune system is unable to mount an adequate immune response."
      },
      "child_count": 40,
      "reference_id": "MONDO:0003778"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 19328,
      "label": "hepatic veno-occlusive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4495
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080177",
          "GARD:0013004",
          "ICD10CM:K76.5",
          "ICD9:453.89",
          "MEDGEN:5514",
          "MESH:D006504",
          "MedDRA:10047216",
          "NCIT:C26793",
          "NORD:879",
          "Orphanet:890",
          "SCTID:65617004",
          "UMLS:C0019156",
          "icd11.foundation:762044088",
          "icd11.foundation:901464792"
        ],
        "synonyms": [
          "Budd Chiari Syndrome",
          "hepatic Vod",
          "liver veno-occlusive disease",
          "sinusoidal obstruction syndrome",
          "veno-occlusive disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Hepatic veno-occlusive disease (hepatic VOD) is a condition resulting from toxic injury to the hepatic sinusoidal capillaries that leads to obstruction of the small hepatic veins."
      },
      "child_count": 1,
      "reference_id": "MONDO:0019514"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5658,
      "label": "inborn error of immunity"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 19328,
      "label": "hepatic veno-occlusive disease"
    }
  ]
}