Hamartomatous polyposis
Symptom Information:
Symptom ID: | HPO:0004390 | |||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Hamartomatous polyposis(HPO:0004390) Neoplasm by histology(HPO:0011792) Hamartoma(HPO:0010566) Hamartomatous polyposis(HPO:0004390) 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) MedDRA: |
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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) |