{
  "id": 18248,
  "label": "familial Mediterranean fever",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018088",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6778,
      "label": "immune system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2914",
          "EFO:0000540",
          "ICD9:279",
          "ICD9:279.1",
          "ICD9:279.10",
          "ICD9:279.19",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:279.8",
          "ICD9:279.9",
          "MEDGEN:5759",
          "MESH:D007154",
          "NANDO:1100004",
          "NANDO:2100202",
          "NCIT:C3507",
          "SCTID:414029004",
          "UMLS:C0021053"
        ],
        "synonyms": [
          "disease of immune system",
          "disease or disorder of immune system",
          "disorder of immune system",
          "immune disease",
          "immune disorder",
          "immune dysfunction",
          "immune system disease or disorder",
          "immune system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from an abnormality in the immune system."
      },
      "child_count": 47,
      "reference_id": "MONDO:0005046"
    },
    {
      "id": 18150,
      "label": "hereditary periodic fever syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16077,
        21247
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021453",
          "MEDGEN:199651",
          "MESH:D056660",
          "Orphanet:324924",
          "UMLS:C0751422"
        ],
        "synonyms": [
          "hereditary periodic fever syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "An instance of periodic fever syndrome that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 12,
      "reference_id": "MONDO:0017953"
    }
  ],
  "children": [
    {
      "id": 8971,
      "label": "familial Mediterranean fever, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18248
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015069",
          "MEDGEN:341987",
          "MESH:C565021",
          "OMIM:134610",
          "UMLS:C1851347"
        ],
        "synonyms": [
          "familial Mediterranean fever, AD",
          "familial Mediterranean fever, autosomal dominant",
          "Fmf, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007601"
    },
    {
      "id": 10793,
      "label": "autosomal recessive familial Mediterranean fever",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7611,
        18248
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009572"
    }
  ],
  "roots": [
    {
      "id": 6778,
      "label": "immune system disorder"
    },
    {
      "id": 18150,
      "label": "hereditary periodic fever syndrome"
    }
  ]
}