Hamartomatous polyposis

Symptom Information:

Symptom ID: HPO:0004390
Synonyms:
GASTROINTESTINAL HAMARTOMATOUS POLYPS [HPO:0004390]
Gastrointestinal hamartomatous polyps [OMIM:Gastrointestinal hamartomatous polyps]
Hamartomatous polyps [OMIM:Hamartomatous polyps]
Gastrointestinal hamartomatous polyps (stomach, small bowel, colon) [OMIM:Gastrointestinal hamartomatous polyps (stomach, small bowel, colon)]
Hamartomatous polyps (stomach to rectum) [OMIM:Hamartomatous polyps (stomach to rectum)]
Quality:
Cross references:
OMIM: "Gastrointestinal hamartomatous polyps" [OMIM:Gastrointestinal hamartomatous polyps]
OMIM: "Hamartomatous polyps" [OMIM:Hamartomatous polyps]
OMIM: "Gastrointestinal hamartomatous polyps (stomach, small bowel, colon)" [OMIM:Gastrointestinal hamartomatous polyps (stomach, small bowel, colon)]
OMIM: "Hamartomatous polyps (stomach to rectum)" [OMIM:Hamartomatous polyps (stomach to rectum)]
Is a (Direct Parents):
HPO         Intestinal polyp
HPO         Hamartoma
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of the intestine(HPO:0002242)
                   Intestinal polyp(HPO:0005266)
                      Hamartomatous polyposis(HPO:0004390)
                Neoplasm of the gastrointestinal tract(HPO:0007378)
                   Intestinal polyp(HPO:0005266)
                      Hamartomatous polyposis(HPO:0004390)
       Neoplasm(HPO:0002664)
          Neoplasm by histology(HPO:0011792)
             Hamartoma(HPO:0010566)
                Hamartomatous polyposis(HPO:0004390)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the gastrointestinal tract(HPO:0007378)
                Intestinal polyp(HPO:0005266)
                   Hamartomatous polyposis(HPO:0004390)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
COWDEN SYNDROME 5 (OMIM:615108)
COWDEN SYNDROME 6 (OMIM:615109)
Cowden syndrome (Orphanet:201)
Cronkhite-Canada syndrome (Orphanet:2930)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
Lhermitte-Duclos disease (Orphanet:65285)
Peutz-Jeghers syndrome (Orphanet:2869)
Proteus-like syndrome (Orphanet:2969)