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58037000: Cowden 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
96476011 Cowden syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
96477019 Multiple hamartoma syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
796725015 Cowden syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1231795010 Cowden's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
96476011 Cowden syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
96477019 Multiple hamartoma syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
96477019 Multiple hamartoma syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
796725015 Cowden syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
796725015 Cowden syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1231795010 Cowden's syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231795010 Cowden's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3439731001000116 Cowden-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
122691000077116 syndrome des hamartomes multiples fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
976371000172115 syndrome de Cowden fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1011741000172115 maladie de Cowden fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
122691000077116 syndrome des hamartomes multiples fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
976371000172115 syndrome de Cowden fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1011741000172115 maladie de Cowden fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3439731001000116 Cowden-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
Cowden syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a Intestinal polyposis syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a Multisystem disorder M-N false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a Familial multiple tumor syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cowden syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a trouble multisytémique false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Associated morphology Neoplasm false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Associated morphology Polyp (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cowden syndrome Finding site Intestinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cowden syndrome Associated morphology Polyp (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cowden syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a Congenital hamartoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cowden syndrome Associated morphology Hamartoma true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cowden syndrome Is a PTEN hamartoma tumour syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cowden syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cowden syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cowden syndrome Is a Congenital anomaly of intestinal tract true Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of Cowden syndrome Associated finding True Cowden syndrome Inferred relationship Existential restriction modifier (core metadata concept) 1
Gingival enlargement due to Cowden syndrome (disorder) Due to True Cowden syndrome Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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