Intestinal polyposis

Symptom Information:

Symptom ID: HPO:0200008
Synonyms:
GASTROINTESTINAL POLYPS [HPO:0200008]
Multiple intestinal polyps [HPO:0200008]
Bowel polyposis [Orphanet:26720]
Gastrointestinal polyps [OMIM:Gastrointestinal polyps]
Multiple intestinal polyps [OMIM:Multiple intestinal polyps]
Polyposis of the bowel/colon/intestine [Orphanet:26720]
Small intestine polyposis [Orphanet:26720]
Quality:
Cross references:
Orphanet:26720 "Polyposis of the bowel/colon/intestine" [Orphanet:26720]
OMIM: "Gastrointestinal polyps" [OMIM:Gastrointestinal polyps]
OMIM: "Multiple intestinal polyps" [OMIM:Multiple intestinal polyps]
Is a (Direct Parents):
HPO         Intestinal polyp
Orphanet Abnormality of the small intestine
Orphanet Adenomatous colonic polyposis
HPO         Large intestinal polyposis
HPO         Small intestinal polyposis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the gastrointestinal tract(HPO:0007378)
                Intestinal polyp(HPO:0005266)
                   Intestinal polyposis(HPO:0200008)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Neoplasm of the gastrointestinal tract(HPO:0007378)
                   Intestinal polyp(HPO:0005266)
                      Intestinal polyposis(HPO:0200008)
                Abnormality of the intestine(HPO:0002242)
                   Intestinal polyp(HPO:0005266)
                      Intestinal polyposis(HPO:0200008)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microdeletion syndrome (Orphanet:276413)
Aicardi syndrome (Orphanet:50)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Cowden syndrome (Orphanet:201)
Cronkhite-Canada syndrome (Orphanet:2930)
Desmoid tumor (Orphanet:873)
Familial adenomatous polyposis (Orphanet:733)
Fibrous dysplasia of bone (Orphanet:249)
Gorlin syndrome (Orphanet:377)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary mixed polyposis syndrome (Orphanet:157794)
Hirschsprung disease (Orphanet:388)
Juvenile polyposis syndrome (Orphanet:2929)
McCune-Albright syndrome (Orphanet:562)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Non-polyposis Turcot syndrome (Orphanet:99817)
POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES (OMIM:175450)
POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL (OMIM:175510)
PTEN hamartoma tumor syndrome (Orphanet:306498)
Peutz-Jeghers syndrome (Orphanet:2869)
Polyostotic fibrous dysplasia (Orphanet:93276)
Proteus-like syndrome (Orphanet:2969)