Adenomatous colonic polyposis

Symptom Information:

Symptom ID: HPO:0005227
Synonyms:
Multiple adenomatous colon polyps [HPO:0005227]
Multiple colonic adenomatous polyps [HPO:0005227]
Colon polyposis [Orphanet:26720]
Adenomatous polyposis coli [HPO:0005227]
Familial multiple polyposis syndrome (disorder) [Orphanet:26720]
Adenomatous polyposis coli (morphologic abnormality) [Orphanet:26720]
Adenomatous Polyposis Coli [Orphanet:26720]
Multiple adenomatous colon polyps [OMIM:Multiple adenomatous colon polyps]
Multiple colonic adenomatous polyps [OMIM:Multiple colonic adenomatous polyps]
Polyposis of the bowel/colon/intestine [Orphanet:26720]
Adenomatous polyposis coli [Orphanet:26720]
Adenomatous polyposis coli [MedDRA:10056981]
Gardner's syndrome [MedDRA:10056981]
Polyposis coli [MedDRA:10056981]
Familial polyposis [MedDRA:10056981]
Familial adenomatous polyposis [MedDRA:10056981]
Small intestine polyposis [Orphanet:26720]
Quality:
Cross references:
Orphanet:26720 "Polyposis of the bowel/colon/intestine" [Orphanet:26720]
OMIM: "Multiple adenomatous colon polyps" [OMIM:Multiple adenomatous colon polyps]
OMIM: "Multiple colonic adenomatous polyps" [OMIM:Multiple colonic adenomatous polyps]
UMLS:C0032580 "Adenomatous Polyposis Coli" [Orphanet:26720]
Is a (Direct Parents):
HPO         Neoplasm of the colon
HPO         Intestinal polyposis
Orphanet Abnormality of the small intestine
MedDRA Intestinal disorders congenital
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)
                Neoplasm of the gastrointestinal tract(HPO:0007378)
                   Neoplasm of the large intestine(HPO:0100834)
                      Neoplasm of the colon(HPO:0100273)
                         Adenomatous colonic polyposis(HPO:0005227)
                   Intestinal polyp(HPO:0005266)
                      Intestinal polyposis(HPO:0200008)
                         Adenomatous colonic polyposis(HPO:0005227)
                Abnormality of the intestine(HPO:0002242)
                   Intestinal polyp(HPO:0005266)
                      Intestinal polyposis(HPO:0200008)
                         Adenomatous colonic polyposis(HPO:0005227)
                   Abnormality of the large intestine(HPO:0002250)
                      Neoplasm of the large intestine(HPO:0100834)
                         Neoplasm of the colon(HPO:0100273)
                            Adenomatous colonic polyposis(HPO:0005227)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the gastrointestinal tract(HPO:0007378)
                Neoplasm of the large intestine(HPO:0100834)
                   Neoplasm of the colon(HPO:0100273)
                      Adenomatous colonic polyposis(HPO:0005227)
                Intestinal polyp(HPO:0005266)
                   Intestinal polyposis(HPO:0200008)
                      Adenomatous colonic polyposis(HPO:0005227)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Intestinal disorders congenital(MedDRA:10022646)
          Adenomatous colonic polyposis(HPO:0005227)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

APC-related attenuated familial adenomatous polyposis (Orphanet:247806)
Attenuated familial adenomatous polyposis (Orphanet:220460)
Familial adenomatous polyposis (Orphanet:733)
Gardner syndrome (Orphanet:79665)
LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER (OMIM:246470)
MUTYH-related attenuated familial adenomatous polyposis (Orphanet:247798)
Oligodontia - cancer predisposition syndrome (Orphanet:300576)
POLYPOSIS SYNDROME, HEREDITARY MIXED, 2 (OMIM:610069)
Turcot syndrome with polyposis (Orphanet:99818)