{
  "id": 22238,
  "label": "autoinflammatory syndrome, familial, Behcet-like",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0031384",
  "properties": {
    "xrefs": [
      "GARD:0025698",
      "OMIMPS:616744"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19503,
      "label": "autoinflammatory syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        7203
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0051000",
          "ICD10CM:M04-M04",
          "MEDGEN:855741",
          "MedDRA:10072220",
          "NANDO:2100156",
          "NCIT:C119050",
          "Orphanet:93665",
          "UMLS:C3890737"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease."
      },
      "child_count": 74,
      "reference_id": "MONDO:0019751"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        5762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:473110",
          "NCIT:C97075",
          "SCTID:363045008",
          "UMLS:C0410787"
        ],
        "synonyms": [
          "Mendelian connective tissue disorder",
          "connective tissue hereditary disorder",
          "hereditary connective tissue disorder",
          "Hereditary Connective Tissue Disorder",
          "Inherited disorder of connective tissue",
          "inherited disorder of connective tissue"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "An inherited genetic disorder that affects the connective tissues. Representative examples include Ehlers-Danlos syndrome and Marfan syndrome."
      },
      "child_count": 176,
      "reference_id": "MONDO:0023603"
    }
  ],
  "children": [
    {
      "id": 21586,
      "label": "autoinflammatory syndrome, familial, X-linked, Behcet-like 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        22238
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025462",
          "MEDGEN:1808082",
          "OMIM:301074",
          "Orphanet:676125",
          "UMLS:C5575495"
        ],
        "synonyms": [
          "AIFBL2",
          "autoinflammatory syndrome, familial, X-linked, Behcet-like 2",
          "deficiency 1n ELF4, X-linked"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0024770"
    },
    {
      "id": 24799,
      "label": "autoinflammatory syndrome, familial, Behcet-like 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        22238
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080944",
          "GARD:0017848",
          "MEDGEN:898541",
          "OMIM:616744",
          "Orphanet:476102",
          "Orphanet:674762",
          "UMLS:C4225218"
        ],
        "synonyms": [
          "AISBL",
          "autoinflammatory syndrome, familial, Behcet-like",
          "Behçet-like disease due to HA20",
          "Behçet-like disease due to haploinsufficiency of A20",
          "autoinflammatory syndrome, familial, Behcet-like 1",
          "hereditary paediatric Behçet-like disease",
          "hereditary pediatric Behçet-like disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0800045"
    }
  ],
  "roots": [
    {
      "id": 19503,
      "label": "autoinflammatory syndrome"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue"
    }
  ]
}