{
  "id": 13109,
  "label": "familial adenomatous polyposis 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012041",
  "properties": {
    "xrefs": [
      "DOID:0080410",
      "GARD:0010805",
      "MEDGEN:474474",
      "MESH:C563924",
      "NCIT:C96520",
      "OMIM:608456",
      "Orphanet:247798",
      "UMLS:C3272841"
    ],
    "synonyms": [
      "FAP2",
      "MAP",
      "MUTYH-associated polyposis",
      "MUTYH-related AFAP",
      "MUTYH-related adenomatous polyposis",
      "adenomas, multiple colorectal, autosomal recessive",
      "colorectal adenomatous polyposis, autosomal recessive",
      "familial adenomatous polyposis 2",
      "familial adenomatous polyposis, 2",
      "familial adenomatous polyposis, type 2",
      "MAP syndrome",
      "MYH-associated polyposis",
      "autosomal recessive familial adenomatous polyposis",
      "autosomal recessive multiple colorectal adenomas"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "An autosomal recessive hereditary cancer predisposition disorder caused by pathogenic variants in the MUTYH gene. It is characterized by an increased risk of colorectal adenomatous polyposis and carcinomas."
  },
  "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": 20300,
      "label": "classic or attenuated familial adenomatous polyposis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16103
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025283"
        ],
        "synonyms": [
          "classic or attenuated FAP",
          "classic or attenuated familial adenomatous polyposis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "An inherited diseases haracterized by the development of adenomas in the rectum and colon; classified into classic FAP and attenuated FAP."
      },
      "child_count": 8,
      "reference_id": "MONDO:0021057"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 20300,
      "label": "classic or attenuated familial adenomatous polyposis"
    }
  ]
}