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72900001: Familial multiple polyposis syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
121087019 Familial multiple polyposis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200309013 Familial adenomatous polyposis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502278019 FPC - Familial polyposis coli en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
502279010 Polyposis coli en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502280013 FAP - Familial adenomatous polyposis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
502281012 Adenomatous polyposis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502282017 Adenomatous polyposis coli en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502283010 APC - Adenomatous polyposis coli en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
502284016 Familial polyposis coli en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
813228015 Familial multiple polyposis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1867561000195110 poliposi adenomatosa familiare it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
323901000172111 syndrome de polypose multiple familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
874081000195110 FAP - Familiäre adenomatöse Polyposis coli de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial multiple polyposis syndrome Is a Autosomal dominant hereditary disorder (disorder) false Inferred relationship Some
Familial multiple polyposis syndrome Is a Digestive system hereditary disorder true Inferred relationship Some
Familial multiple polyposis syndrome Is a Intestinal polyposis syndrome true Inferred relationship Some
Familial multiple polyposis syndrome Is a Disorder of large intestine false Inferred relationship Some
Familial multiple polyposis syndrome Is a Familial disease false Inferred relationship Some
Familial multiple polyposis syndrome Finding site Structure of large intestine (body structure) false Inferred relationship Some 2
Familial multiple polyposis syndrome Associated morphology Multiple polyps false Inferred relationship Some 2
Familial multiple polyposis syndrome Finding site Intestinal structure false Inferred relationship Some 1
Familial multiple polyposis syndrome Is a Hereditary disorder of the integument false Inferred relationship Some
Familial multiple polyposis syndrome Is a Familial multiple tumor syndrome false Inferred relationship Some
Familial multiple polyposis syndrome Is a Polyp of large intestine (disorder) true Inferred relationship Some
Familial multiple polyposis syndrome Associated morphology Neoplasm false Inferred relationship Some
Familial multiple polyposis syndrome Associated morphology anomalie congénitale false Inferred relationship Some
Familial multiple polyposis syndrome Finding site Skin structure false Inferred relationship Some
Familial multiple polyposis syndrome Occurrence Congenital false Inferred relationship Some
Familial multiple polyposis syndrome Associated morphology Multiple polyps true Inferred relationship Some 1
Familial multiple polyposis syndrome Finding site Structure of large intestine (body structure) true Inferred relationship Some 1
Familial multiple polyposis syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Gardner syndrome (disorder) Is a True Familial multiple polyposis syndrome Inferred relationship Some
Turcot syndrome Is a True Familial multiple polyposis syndrome Inferred relationship Some
Family history of familial multiple polyposis syndrome (situation) Associated finding True Familial multiple polyposis syndrome Inferred relationship Some 1
A mild form of familial adenomatous polyposis characterized by the presence of fewer than 100 adenomatous colonic polyps, a more proximal colonic location, a delayed age of colorectal cancer onset and a more limited expression of the extracolonic features. Is a True Familial multiple polyposis syndrome Inferred relationship Some
A rare, genetic intestinal disease characterized by the presence of multiple (usually large) hyperplastic/serrated colorectal polyps, usually with a pancolonic distribution. Histology reveals hyperplastic polyps, sessile serrated adenomas (most common), traditional serrated adenomas or mixed polyps. It is associated with an increased personal and familial (first-degree relatives) risk of colorectal cancer. Is a True Familial multiple polyposis syndrome Inferred relationship Some
Familial adenomatous polyposis due to 5q22.2 microdeletion (disorder) Is a True Familial multiple polyposis syndrome Inferred relationship Some
Malignant neoplasm of intestine due to familial adenomatous polyposis (disorder) Due to True Familial multiple polyposis syndrome Inferred relationship Some 2

This concept is not in any reference sets

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