{
  "id": 10793,
  "label": "autosomal recessive familial Mediterranean fever",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009572",
  "properties": {
    "xrefs": [
      "GARD:0024682",
      "NANDO:1200864",
      "OMIM:249100"
    ],
    "synonyms": [
      "autosomal recessive familial Mediterranean fever",
      "familial Mediterranean fever, AR",
      "familial Mediterranean fever, autosomal recessive",
      "FMF",
      "familial MEDITERRANEAN FEVER",
      "familial Mediterranean fever",
      "polyserositis, familial paroxysmal",
      "polyserositis, recurrent"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "Autosomal recessive form of familial Mediterranean fever."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    },
    {
      "id": 18248,
      "label": "familial Mediterranean fever",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778,
        18150
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2987",
          "GARD:0006421",
          "ICD9:277.31",
          "MEDGEN:45811",
          "MESH:D010505",
          "MedDRA:10016207",
          "NANDO:1200863",
          "NANDO:2200431",
          "NCIT:C84707",
          "NORD:1130",
          "Orphanet:342",
          "SCTID:12579009",
          "UMLS:C0031069",
          "icd11.foundation:1373335705"
        ],
        "synonyms": [
          "FMF",
          "Fiebre mediterránea familiar",
          "benign paroxysmal peritonitis",
          "benign recurrent polyserositis",
          "familial paroxysmal polyserositis",
          "periodic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles."
      },
      "child_count": 4,
      "reference_id": "MONDO:0018088"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 18248,
      "label": "familial Mediterranean fever"
    }
  ]
}