{
  "id": 2848,
  "label": "multinodular goiter",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000334",
  "properties": {
    "xrefs": [
      "DOID:0050489",
      "MEDGEN:87431",
      "NCIT:C131438",
      "OMIMPS:138800",
      "SCTID:237570007",
      "UMLS:C0342208"
    ],
    "synonyms": [
      "goiter, multinodular"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Nodular goiter characterized by more than one discrete tissue mass."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 8310,
      "label": "nodular goiter",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7075
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13197",
          "EFO:1001062",
          "HP:0005994",
          "MEDGEN:42271",
          "MESH:D006044",
          "MedDRA:10018495",
          "NCIT:C131437",
          "SCTID:419153005",
          "UMLS:C0018023"
        ],
        "synonyms": [
          "goiter, nodular",
          "nodular goiter",
          "nodular goiter (disease)",
          "nodular goitre (disease)",
          "nodular goitre NOS"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Goiter characterized by discrete tissue mass(es) that may or may not produce thyroid hormones."
      },
      "child_count": 1,
      "reference_id": "MONDO:0006869"
    }
  ],
  "children": [
    {
      "id": 9038,
      "label": "goiter, multinodular 1, with or without Sertoli-Leydig cell tumors",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2848,
        16218,
        23957
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017278",
          "ICD9:240.0",
          "MEDGEN:86230",
          "MESH:C562732",
          "OMIM:138800",
          "Orphanet:276399",
          "SCTID:267369002",
          "UMLS:C0302859"
        ],
        "synonyms": [
          "euthyroid goiter",
          "euthyroid goitre",
          "simple goiter",
          "simple goitre",
          "FMNG",
          "MNG1",
          "familial MNG",
          "goiter, multinodular 1, with or without Sertoli-Leydig cell tumors",
          "goiter, nontoxic, with Intrathyroidal calcification",
          "multinodular goiter, adolescent"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any multinodular goiter in which the cause of the disease is a mutation in the DICER1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007681"
    },
    {
      "id": 11463,
      "label": "goiter, multinodular 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2848
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:337370",
          "MESH:C564546",
          "OMIM:300273",
          "UMLS:C1846033"
        ],
        "synonyms": [
          "MNG2",
          "goiter, multinodular 2",
          "goiter, multinodular, 2, X-linked dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010290"
    },
    {
      "id": 12730,
      "label": "goiter, multinodular 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2848
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:342940",
          "MESH:C565260",
          "OMIM:606082",
          "UMLS:C1853686"
        ],
        "synonyms": [
          "MNG3",
          "goiter, multinodular 3",
          "goiter, multinodular, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011635"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 8310,
      "label": "nodular goiter"
    }
  ]
}