Intestinal polyposis
Symptom Information:
Symptom ID: | HPO:0200008 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
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) Intestinal polyp(HPO:0005266) Intestinal polyposis(HPO:0200008) Abnormality of the intestine(HPO:0002242) Intestinal polyp(HPO:0005266) Intestinal polyposis(HPO:0200008) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the gastrointestinal tract(HPO:0007378) 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) |