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60876000: Gardner syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
101150018 Gardner syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
799876013 Gardner syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232143012 GS - Gardner's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
101150018 Gardner syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
799876013 Gardner syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
799876013 Gardner syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232143012 GS - Gardner's syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232143012 GS - Gardner's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1043671000195117 sindrome di Gardner it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
655081000274115 Familiäre multiple Polyposis de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3455271001000114 Gardner-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
122741000077118 syndrome de Gardner fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
122741000077118 syndrome de Gardner fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1043671000195117 sindrome di Gardner it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
655081000274115 Familiäre multiple Polyposis de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3455271001000114 Gardner-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

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 (core metadata concept)
Gardner syndrome Is a Multisystem disorder G-H false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Finding site Structure of large intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Gardner syndrome Associated morphology Multiple polyps false Inferred relationship Existential restriction modifier (core metadata concept) 1
Gardner syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Is a trouble multisytémique false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Gardner syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Associated morphology Neoplasm false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Associated morphology Multiple polyps true Inferred relationship Existential restriction modifier (core metadata concept) 1
Gardner syndrome Finding site Structure of large intestine (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Gardner syndrome Is a Congenital hamartoma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Gardner syndrome Associated morphology Hamartoma true Inferred relationship Existential restriction modifier (core metadata concept) 2
Gardner syndrome Is a Congenital anomaly of large intestine (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Gardner syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Gardner syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Gardner syndrome Is a Hamartoma of intestine true Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Finding site Structure of large intestine (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Gardner syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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