{
  "id": 21586,
  "label": "autoinflammatory syndrome, familial, X-linked, Behcet-like 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024770",
  "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"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22238,
      "label": "autoinflammatory syndrome, familial, Behcet-like",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19503,
        21247
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025698",
          "OMIMPS:616744"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0031384"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22238,
      "label": "autoinflammatory syndrome, familial, Behcet-like"
    }
  ]
}