60876000: Gardner syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Bowel finding\...

\Finding of large intestine\Disorder of large intestine\...

\Polyp of large intestine\Familial multiple polyposis syndrome\Gardner syndrome

\Congenital anomaly of large intestine\Gardner syndrome

\Disorder of intestine\Hamartoma of intestine\Gardner syndrome
\Disorder of intestine\Polyp of intestine\Polyp of large intestine\Familial multiple polyposis syndrome\Gardner syndrome
\Disorder of intestine\Polyp of intestine\Intestinal polyposis syndrome\Familial multiple polyposis syndrome\Gardner syndrome
\Disorder of intestine\Congenital anomaly of intestinal tract\Congenital anomaly of large intestine\Gardner syndrome
\Disorder of intestine\Disorder of large intestine\Polyp of large intestine\Familial multiple polyposis syndrome\Gardner syndrome
\Disorder of intestine\Disorder of large intestine\Congenital anomaly of large intestine\Gardner syndrome

\Mass of body structure\Mass of body region\Mass of trunk\Abdominal mass\Hamartoma of intestine\Gardner syndrome
\Mass of body structure\Mass of body region\Mass of trunk\Abdominal mass\Polyp of intestine\Polyp of large intestine\Familial multiple polyposis syndrome\Gardner syndrome
\Mass of body structure\Mass of body region\Mass of trunk\Abdominal mass\Polyp of intestine\Intestinal polyposis syndrome\Familial multiple polyposis syndrome\Gardner syndrome
\Mass of body structure\Mass of digestive structure\Hamartoma of intestine\Gardner syndrome
\Mass of body structure\Mass of digestive structure\Polyp of intestine\Polyp of large intestine\Familial multiple polyposis syndrome\Gardner syndrome
\Mass of body structure\Mass of digestive structure\Polyp of intestine\Intestinal polyposis syndrome\Familial multiple polyposis syndrome\Gardner syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

101150018 Gardner syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

799876013 Gardner syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

1232143012 GS - Gardner's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Gardner syndrome	Is a	Familial multiple polyposis syndrome	true	Inferred relationship	Existential restriction modifier
Gardner syndrome	Is a	Multisystem disorder G-H	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Is a	Congenital hamartosis	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Finding site	Structure of large intestine	false	Inferred relationship	Existential restriction modifier	1
Gardner syndrome	Associated morphology	Multiple polyps	false	Inferred relationship	Existential restriction modifier	1
Gardner syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Is a	Multisystem disorder	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Finding site	Intestinal structure	false	Inferred relationship	Existential restriction modifier	1
Gardner syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Associated morphology	Hamartoma	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Associated morphology	Neoplasm	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier
Gardner syndrome	Associated morphology	Multiple polyps	true	Inferred relationship	Existential restriction modifier	1
Gardner syndrome	Finding site	Structure of large intestine	true	Inferred relationship	Existential restriction modifier	1
Gardner syndrome	Is a	Congenital hamartoma	true	Inferred relationship	Existential restriction modifier
Gardner syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Gardner syndrome	Associated morphology	Hamartoma	true	Inferred relationship	Existential restriction modifier	2
Gardner syndrome	Is a	Congenital anomaly of large intestine	true	Inferred relationship	Existential restriction modifier
Gardner syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Gardner syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Gardner syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	2
Gardner syndrome	Is a	Hamartoma of intestine	true	Inferred relationship	Existential restriction modifier
Gardner syndrome	Finding site	Structure of large intestine	true	Inferred relationship	Existential restriction modifier	2
Gardner syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
101150018	Gardner syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
799876013	Gardner syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
1232143012	GS - Gardner's syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module