{
  "id": 16342,
  "label": "congenital epulis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015528",
  "properties": {
    "xrefs": [
      "DOID:7280",
      "DOID:8303",
      "GARD:0020016",
      "MEDGEN:83962",
      "MESH:D005887",
      "NCIT:C4675",
      "Orphanet:157826",
      "SCTID:360525006",
      "UMLS:C0376319",
      "icd11.foundation:1616915738"
    ],
    "synonyms": [
      "Neumann tumor",
      "Neumann tumour",
      "congenital epulis",
      "congenital gingival cell tumor",
      "congenital gingival cell tumour",
      "congenital granular cell tumor",
      "congenital granular cell tumour",
      "gingival granular cell tumor",
      "gingival granular cell tumour"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "A congenital gingival tumor that occurs along the alveolar ridge of the maxilla. It usually affects female infants. The histogenesis is unknown. Morphologically, it is characterized by the presence of large cells with eosinophilic granular cytoplasm. Complete surgical resection is curative."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    },
    {
      "id": 5328,
      "label": "epulis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4579,
        6807
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5337",
          "ICD9:523.8",
          "MEDGEN:82751",
          "NCIT:C3948",
          "SCTID:45676007",
          "UMLS:C0266919",
          "icd11.foundation:1849228776"
        ],
        "synonyms": [
          "gingiva polyp",
          "gingival polyp",
          "gum polyp",
          "polyp of gingiva",
          "polyp of gum",
          "polyp of the gingiva",
          "polyp of the gum"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A non-neoplastic nodular lesion that arises from the gingiva."
      },
      "child_count": 4,
      "reference_id": "MONDO:0003396"
    },
    {
      "id": 7788,
      "label": "granular cell tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4613
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2411",
          "EFO:1000284",
          "GARD:0009618",
          "ICD9:215.9",
          "ICDO:9580/0",
          "MEDGEN:88345",
          "MESH:C535558",
          "MESH:D016586",
          "NCIT:C3474",
          "ONCOTREE:GCT",
          "SCTID:404035005",
          "UMLS:C0085167"
        ],
        "synonyms": [
          "Abrikossoff tumor",
          "Abrikossoff tumour",
          "Abrikossoff's tumor",
          "Abrikossoff's tumour",
          "granular cell myoblastoma",
          "granular cell neoplasm",
          "granular cell nerve sheath tumor",
          "granular cell nerve sheath tumour",
          "granular cell schwannoma",
          "granular cell tumor",
          "granular cell tumor (morphologic abnormality)",
          "granular cell tumour (morphologic abnormality)",
          "granular cell tumor NOS (morphologic abnormality)",
          "granular cell tumour NOS (morphologic abnormality)",
          "neoplasm of granular cell",
          "Abrikosoff's granulous cell tumor",
          "Abrikosoff's granulous cell tumour",
          "Abrikosoff's tumor",
          "Abrikosoff's tumour",
          "Abrikosov's tumor",
          "Abrikosov's tumour",
          "Abrikosov’s tumor",
          "Abrikosov’s tumour",
          "GCT",
          "giant granulocellular Abrikosov's tumor",
          "giant granulocellular Abrikosov's tumour",
          "malignant variant of Abrikosov's tumor",
          "malignant variant of Abrikosov's tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An unusual benign or malignant neoplasm characterized by the presence of neoplastic large polygonal cells with granular, eosinophilic cytoplasm which contains abundant lysosomes. It was originally thought to be a tumor originating from muscle cells and was named granular cell myoblastoma. Subsequent studies have suggested a derivation from Schwann cells. It affects females more often than males and it usually presents as a solitary mass. A minority of patients have multiple tumors. It can arise from many anatomic sites including the posterior pituitary gland, skin, oral cavity, esophagus, stomach, heart, mediastinum, and breast."
      },
      "child_count": 9,
      "reference_id": "MONDO:0006235"
    },
    {
      "id": 7941,
      "label": "soft tissue neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23336
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000541",
          "MEDGEN:11495",
          "NCIT:C3377",
          "ONCOTREE:SOFT_TISSUE",
          "SCTID:387837005",
          "UMLS:C0037579"
        ],
        "synonyms": [
          "neoplasm of soft tissue",
          "neoplasm of the soft tissue",
          "soft tissue neoplasm",
          "soft tissue tumor",
          "soft tissue tumors",
          "soft tissue tumour",
          "soft tissue tumours",
          "tumor of soft tissue",
          "tumor of the soft tissue",
          "tumour of soft tissue",
          "tumour of the soft tissue",
          "SOFT_TISSUE"
        ],
        "definition": "A benign, intermediate, or malignant neoplasm that arises from the soft tissue. The most common types are lipomatous (fatty), vascular, smooth muscle, fibrous, and fibrohistiocytic neoplasms."
      },
      "child_count": 18,
      "reference_id": "MONDO:0006424"
    },
    {
      "id": 7993,
      "label": "hamartoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6798
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3462",
          "EFO:1000634",
          "HP:0010566",
          "ICD9:759.6",
          "MEDGEN:6713",
          "MESH:D006222",
          "NCIT:C3075",
          "SCTID:400006008",
          "UMLS:C0018552"
        ],
        "synonyms": [
          "hamartoma",
          "hamartoma (disease)"
        ],
        "definition": "A benign and excessive tumor-like growth of mature cells and normal tissues which grow in a disorganized pattern."
      },
      "child_count": 13,
      "reference_id": "MONDO:0006499"
    },
    {
      "id": 20327,
      "label": "gingival neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4170,
        7231,
        20434
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:6605",
          "NCIT:C3057",
          "SCTID:126792007",
          "UMLS:C0017570"
        ],
        "synonyms": [
          "gingiva neoplasm",
          "gingiva neoplasm (disease)",
          "gingiva tumor",
          "gingiva tumour",
          "gingival neoplasm",
          "gingival tumor",
          "gingival tumour",
          "gum neoplasm",
          "gum tumor",
          "gum tumour",
          "neoplasm of gingiva",
          "neoplasm of gum",
          "neoplasm of the gingiva",
          "neoplasm of the gum",
          "tumor of gingiva",
          "tumor of gum",
          "tumor of the gingiva",
          "tumor of the gum",
          "tumour of gingiva",
          "tumour of gum",
          "tumour of the gingiva",
          "tumour of the gum"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A benign or malignant neoplasm that affects the upper or lower gingiva."
      },
      "child_count": 9,
      "reference_id": "MONDO:0021086"
    },
    {
      "id": 20677,
      "label": "neoplasm of jaw",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8301,
        20434,
        21213,
        21561
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025339",
          "ICD9:239.89",
          "MEDGEN:43991",
          "SCTID:126634001",
          "UMLS:C0022364"
        ],
        "synonyms": [
          "jaw skeleton neoplasm",
          "jaw skeleton neoplasm (disease)",
          "jaw skeleton tumor",
          "jaw skeleton tumour",
          "neoplasm of jaw skeleton",
          "tumor of jaw skeleton",
          "tumour of jaw skeleton"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A neoplasm (disease) that involves the jaw skeleton."
      },
      "child_count": 20,
      "reference_id": "MONDO:0021580"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 5328,
      "label": "epulis"
    },
    {
      "id": 7788,
      "label": "granular cell tumor"
    },
    {
      "id": 7941,
      "label": "soft tissue neoplasm"
    },
    {
      "id": 7993,
      "label": "hamartoma"
    },
    {
      "id": 20327,
      "label": "gingival neoplasm"
    },
    {
      "id": 20677,
      "label": "neoplasm of jaw"
    }
  ]
}