{
  "id": 17689,
  "label": "juvenile polyposis syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017380",
  "properties": {
    "xrefs": [
      "GARD:0003065",
      "MEDGEN:87518",
      "NANDO:2200916",
      "NCIT:C7754",
      "NORD:280170",
      "OMIM:174900",
      "Orphanet:2929",
      "SCTID:9273005",
      "UMLS:C0345893",
      "icd11.foundation:1020795563"
    ],
    "synonyms": [
      "JIP",
      "JPS",
      "jPS",
      "juvenile gastrointestinal polyposis",
      "juvenile intestinal polyposis",
      "juvenile multiple polyps syndrome",
      "juvenile polyposis",
      "juvenile polyposis syndrome",
      "polyposis, juvenile intestinal",
      "PJI",
      "polyposis familial of entire gastrointestinal tract",
      "polyposis juvenile intestinal"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Juvenile gastrointestinal polyposis (JIP) is a rare condition characterized by the presence of juvenile hamartomatous polyps in the gastrointestinal (GI) tract."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 6151,
      "label": "digestive system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:77",
          "ICD10CM:K00-K95",
          "ICD9:520-579",
          "ICD9:V47.3",
          "MEDGEN:892790",
          "MESH:D005767",
          "NANDO:1100013",
          "NCIT:C2990",
          "SCTID:53619000",
          "UMLS:C4023588",
          "icd11.foundation:1256772020"
        ],
        "synonyms": [
          "digestive disease",
          "digestive system disease",
          "digestive system disease or disorder",
          "digestive system disorder",
          "disease of digestive system",
          "disease or disorder of digestive system",
          "disorder of digestive system",
          "gastroenterological system disease",
          "gastroenterological system disorder",
          "gastrointestinal disorder",
          "gastrointestinal system disease",
          "gastrointestinal system disorder",
          "stomach or intestinal disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease or disorder that involves the digestive system."
      },
      "child_count": 31,
      "reference_id": "MONDO:0004335"
    },
    {
      "id": 16103,
      "label": "intestinal polyposis syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019847",
          "MEDGEN:577190",
          "MedDRA:10057018",
          "NCIT:C155954",
          "Orphanet:104010",
          "SCTID:254589009",
          "UMLS:C0345891"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A syndrome associated with the development of multiple polyps throughout the intestine. It includes familial adenomatous polyposis , hamartomatous polyposis syndromes, and other rare polyposis syndromes."
      },
      "child_count": 8,
      "reference_id": "MONDO:0015185"
    }
  ],
  "children": [
    {
      "id": 9583,
      "label": "generalized juvenile polyposis/juvenile polyposis coli",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2903,
        17689
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050787",
          "GARD:0017508",
          "MEDGEN:356898",
          "Orphanet:329971",
          "UMLS:C1868081"
        ],
        "synonyms": [
          "generalized juvenile polyposis/juvenile polyposis coli",
          "jPS",
          "juvenile intestinal polyposis",
          "juvenile polyposis coli",
          "juvenile polyposis of stomach",
          "juvenile polyposis syndrome",
          "polyposis, familial, of Entire gastrointestinal tract",
          "polyposis, juvenile intestinal"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0008276"
    },
    {
      "id": 19060,
      "label": "juvenile polyposis of infancy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17689
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016696",
          "MEDGEN:1778573",
          "Orphanet:79076",
          "UMLS:C5445164",
          "icd11.foundation:378686036"
        ],
        "synonyms": [
          "infantile juvenile polyposis syndrome",
          "infantile onset juvenile polyposis syndrome",
          "juvenile polyposis syndrome of infancy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Juvenile polyposis of infancy (JPI) is the most severe form of juvenile gastrointestinal polyposis and is characterized by pancolonic hamartomatous polyposis from stomach to rectum, diagnosed in the first two years of life."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019190"
    },
    {
      "id": 24722,
      "label": "BMPR1A-related juvenile polyposis syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2903,
        17689
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0028022"
        ],
        "synonyms": [
          "BMPR1A-related juvenile polyposis syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "An autosomal dominant disorder caused by pathogenic variants in the BMPR1A gene characterized by gastrointestinal juvenile polyps and a predisposition to gastrointestinal cancer."
      },
      "child_count": 0,
      "reference_id": "MONDO:0700348"
    }
  ],
  "roots": [
    {
      "id": 6151,
      "label": "digestive system disorder"
    },
    {
      "id": 16103,
      "label": "intestinal polyposis syndrome"
    }
  ]
}