loading...| Preferred Name | familial adenomatous polyposis 1 | |
| Synonyms |
adenomatous polyposis of the colon polyposis, adenomatous intestinal familial adenomatous polyposis, attenuated Gardner syndrome brain tumor-polyposis syndrome 2 familial polyposis of the colon adenomatous polyposis coli, attenuated adenomatous polyposis coli adenoma, periampullary, somatic FAP1 attenuated familial adenomatous polyposis caused by mutation in APC familial adenomatous polyposis 1 APC attenuated familial adenomatous polyposis |
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| Definitions |
Any attenuated familial adenomatous polyposis in which the cause of the disease is a mutation in the APC gene. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0021056 |
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| altLabel |
adenomatous polyposis of the colon polyposis, adenomatous intestinal familial adenomatous polyposis, attenuated Gardner syndrome brain tumor-polyposis syndrome 2 familial polyposis of the colon adenomatous polyposis coli, attenuated adenomatous polyposis coli adenoma, periampullary, somatic FAP1 attenuated familial adenomatous polyposis caused by mutation in APC familial adenomatous polyposis 1 APC attenuated familial adenomatous polyposis |
|
| definition |
Any attenuated familial adenomatous polyposis in which the cause of the disease is a mutation in the APC gene. |
|
| has_broad_synonym |
adenomatous polyposis coli |
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| has_exact_synonym |
adenoma, periampullary, somatic FAP1 attenuated familial adenomatous polyposis caused by mutation in APC familial adenomatous polyposis 1 APC attenuated familial adenomatous polyposis |
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| has_related_synonym |
adenomatous polyposis of the colon polyposis, adenomatous intestinal familial adenomatous polyposis, attenuated Gardner syndrome brain tumor-polyposis syndrome 2 familial polyposis of the colon adenomatous polyposis coli, attenuated |
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| IAO_0000233 | ||
| label |
familial adenomatous polyposis 1 |
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| prefixIRI |
MONDO:0021056 |
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| prefLabel |
familial adenomatous polyposis 1 |
|
| textual definition |
Any attenuated familial adenomatous polyposis in which the cause of the disease is a mutation in the APC gene. |
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| subClassOf |