{
  "id": 2772,
  "label": "autoimmune disease, multisystem, infantile-onset",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000213",
  "properties": {
    "xrefs": [
      "DOID:0061159",
      "OMIMPS:615952"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "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": 8586,
      "label": "autoimmune disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:417",
          "EFO:0005809",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:720",
          "MEDGEN:2135",
          "MESH:D001327",
          "NCIT:C2889",
          "OBI:1110054",
          "OMIM:109100",
          "SCTID:85828009",
          "UMLS:C0004364"
        ],
        "synonyms": [
          "autoimmune disease",
          "autoimmune disease or disorder",
          "autoimmune disorder",
          "disease, autoimmune",
          "autoimmune hypersensitivity disease",
          "hypersensitivity reaction type II disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis)."
      },
      "child_count": 47,
      "reference_id": "MONDO:0007179"
    }
  ],
  "children": [
    {
      "id": 15416,
      "label": "STAT3-related early-onset multisystem autoimmune disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2772,
        4440
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061160",
          "GARD:0017737",
          "MEDGEN:863232",
          "NCIT:C157123",
          "OMIM:615952",
          "Orphanet:438159",
          "UMLS:C4014795"
        ],
        "synonyms": [
          "ADMIO",
          "ADMIO1",
          "autoimmune disease, multisystem, infantile-onset",
          "autoimmune disease, multisystem, infantile-onset, 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014414"
    },
    {
      "id": 15843,
      "label": "autoimmune disease, multisystem, infantile-onset, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2772
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061161",
          "MEDGEN:934735",
          "OMIM:617006",
          "UMLS:C4310768"
        ],
        "synonyms": [
          "ADMIO2",
          "ZAP70 autoimmune disease, multisystem, infantile-onset",
          "autoimmune disease, multisystem, infantile-onset caused by mutation in ZAP70",
          "autoimmune disease, multisystem, infantile-onset, 2",
          "autoimmune disease, multisystem, infantile-onset, 2; ADMIO2",
          "autoimmune disease, multisystem, infantile-onset, type 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any autoimmune disease, multisystem, infantile-onset in which the cause of the disease is a mutation in the ZAP70 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014861"
    },
    {
      "id": 25660,
      "label": "autoimmune disease, multisystem, infantile-onset, 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2772
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061162",
          "MEDGEN:1841236",
          "OMIM:620430",
          "UMLS:C5830600"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957388"
    },
    {
      "id": 26244,
      "label": "autoimmune disease, multisystem, infantile-onset, 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2772
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061164",
          "MEDGEN:1876460",
          "OMIM:621235",
          "UMLS:C6012737"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0979235"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 8586,
      "label": "autoimmune disease"
    }
  ]
}