{
  "id": 6463,
  "label": "primary thrombocytopenia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004680",
  "properties": {
    "xrefs": [
      "DOID:8925",
      "GARD:0024085",
      "ICD9:287.3",
      "ICD9:287.30",
      "ICD9:287.39",
      "MEDGEN:675208",
      "SCTID:267534000",
      "UMLS:C0701157"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 3016,
      "label": "autoimmune disorder of blood",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7217,
        8586
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060050"
        ],
        "synonyms": [
          "blood autoimmune disease",
          "blood hypersensitivity reaction type II disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A hypersensitivity reaction type II disease that involves the blood."
      },
      "child_count": 4,
      "reference_id": "MONDO:0000602"
    }
  ],
  "children": [
    {
      "id": 9845,
      "label": "autoimmune thrombocytopenic purpura",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6463,
        18985,
        23244
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8924",
          "EFO:0007160",
          "GARD:0005194",
          "ICD10CM:D69.3",
          "ICD9:287.31",
          "MEDGEN:584986",
          "MedDRA:10021245",
          "NANDO:1200315",
          "NANDO:2200645",
          "NCIT:C3446",
          "OMIM:188030",
          "Orphanet:3002",
          "UMLS:C0398650",
          "icd11.foundation:364346400"
        ],
        "synonyms": [
          "immune thrombocytopenia",
          "ITP",
          "autoimmune thrombocytopenic purpura",
          "idiopathic thrombocytopenia",
          "idiopathic thrombocytopenia purpura",
          "idiopathic thrombocytopenic purpura",
          "thrombocytopenic purpura, autoimmune",
          "AITP",
          "immune thrombocytopenic purpura",
          "thrombocytopenic purpura autoimmune"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An autoimmune disorder in which the number of circulating platelets is reduced due to their antibody-mediated destruction. ITP is a diagnosis of exclusion and is heterogeneous in origin."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008558"
    },
    {
      "id": 16668,
      "label": "Evans syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        6463,
        18985,
        19736
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8931",
          "GARD:0006389",
          "ICD10CM:D69.41",
          "ICD9:287.32",
          "MEDGEN:75773",
          "MESH:C536380",
          "MedDRA:10053873",
          "NANDO:1200310",
          "NCIT:C61284",
          "NORD:1112",
          "Orphanet:1959",
          "SCTID:75331009",
          "UMLS:C0272126",
          "icd11.foundation:1048228553"
        ],
        "synonyms": [
          "Evans' syndrome",
          "autoimmune hemolytic anaemia and autoimmune thrombocytopenia",
          "autoimmune hemolytic anemia and autoimmune thrombocytopenia",
          "immune pancytopenia",
          "Evan syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Evans syndrome is a rare chronic hematologic disorder characterized by the simultaneous or sequential association of autoimmune hemolytic anemia (AIHA; a disorder in which auto-antibodies are directed against red blood cells causing anemia of varying degrees of severity) with immune thrombocytopenic purpura (ITP; a coagulation disorder in which auto-antibodies are directed against platelets causing hemorrhagic episodes) and occasionally autoimmune neutropenia, in the absence of a known underlying etiology."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016030"
    }
  ],
  "roots": [
    {
      "id": 3016,
      "label": "autoimmune disorder of blood"
    }
  ]
}