{
  "id": 13600,
  "label": "multiple endocrine neoplasia type 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012552",
  "properties": {
    "xrefs": [
      "DOID:0080137",
      "GARD:0017275",
      "MEDGEN:373469",
      "MESH:C567059",
      "NCIT:C157449",
      "OMIM:610755",
      "Orphanet:276152",
      "SCTID:715907003",
      "UMLS:C1970712",
      "icd11.foundation:157945677"
    ],
    "synonyms": [
      "CDKN1B multiple endocrine neoplasia",
      "MEN4",
      "multiple endocrine neoplasia caused by mutation in CDKN1B",
      "multiple endocrine neoplasia type 4",
      "multiple endocrine neoplasia, type IV",
      "multiple endocrine neoplasia, type 4"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 17512,
      "label": "multiple endocrine neoplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16050,
        16218,
        20691
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3125",
          "GARD:0021044",
          "ICD10CM:E31.2",
          "ICD9:258.0",
          "ICDO:8360/1",
          "MEDGEN:45036",
          "MESH:D009377",
          "MedDRA:10061299",
          "NANDO:2100148",
          "NCIT:C6432",
          "OMIMPS:131100",
          "Orphanet:276161",
          "SCTID:46724008",
          "UMLS:C0027662"
        ],
        "synonyms": [
          "MEN",
          "men syndrome",
          "men syndromes",
          "multiple endocrine adenomatosis",
          "multiple endocrine neoplasia",
          "multiple endocrine neoplasia syndrome",
          "multiple endocrine neoplasia syndrome(s)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs."
      },
      "child_count": 9,
      "reference_id": "MONDO:0017169"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 17512,
      "label": "multiple endocrine neoplasia"
    }
  ]
}