{
  "id": 14785,
  "label": "autoimmune lymphoproliferative syndrome type 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013767",
  "properties": {
    "xrefs": [
      "DOID:0110117",
      "GARD:0017262",
      "MEDGEN:382434",
      "OMIM:614470",
      "Orphanet:268114",
      "SCTID:723508002",
      "UMLS:C2674723"
    ],
    "synonyms": [
      "ALPS4",
      "NRAS autoimmune lymphoproliferative syndrome",
      "RALD",
      "RAS-associated autoimmune leukoproliferative disease",
      "RAS-associated autoimmune leukoproliferative disorder",
      "RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic",
      "autoimmune lymphoproliferative syndrome caused by mutation in NRAS",
      "autoimmune lymphoproliferative syndrome, type 4"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "RAS-associated autoimmune leukoproliferative disease (RALD) is a rare genetic disorder characterized by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinemia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18157,
      "label": "autoimmune lymphoproliferative syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4539,
        8586,
        17033,
        20301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "CSP:1560-5548",
          "DOID:6688",
          "GARD:0008686",
          "ICD10CM:D89.82",
          "MESH:D056735",
          "MedDRA:10069521",
          "NANDO:1200352",
          "NANDO:2200726",
          "NCIT:C37864",
          "Orphanet:3261",
          "icd11.foundation:1072688797"
        ],
        "synonyms": [
          "ALPS",
          "ALPS (autoimmune lymphoproliferative syndrome)",
          "Canale-Smith syndrome",
          "FAS deficiency",
          "autoimmune lymphoproliferative syndrome type 1, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Autoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder characterized by non-malignant lymphoproliferation, multilineage cytopenias, and a lifelong increased risk of Hodgkin's and non-Hodgkin's lymphoma."
      },
      "child_count": 36,
      "reference_id": "MONDO:0017979"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18157,
      "label": "autoimmune lymphoproliferative syndrome"
    }
  ]
}