FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

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
1011741000172115 maladie de Cowden fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
122691000077116 syndrome des hamartomes multiples fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
1231795010 Cowden's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
394931000077117 syndrome des hamartomes multiples (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
796725015 Cowden syndrome (disorder) en Fully specified name 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 Entire term case insensitive (core metadata concept) SNOMED CT core
976371000172115 syndrome de Cowden fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
syndrome des hamartomes multiples (trouble) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Congenital anomaly of intestinal tract true Inferred relationship Some
syndrome des hamartomes multiples (trouble) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Multisystem disorder (disorder) false Inferred relationship Some
syndrome des hamartomes multiples (trouble) morphologie associée (attribut) Neoplasm false Inferred relationship Some
syndrome des hamartomes multiples (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
syndrome des hamartomes multiples (trouble) morphologie associée (attribut) polype false Inferred relationship Some 1
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Congenital anomaly of trunk false Inferred relationship Some
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Congenital anomaly of digestive system false Inferred relationship Some
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Congenital hamartosis false Inferred relationship Some
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Intestinal polyposis syndrome true Inferred relationship Some
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Multisystem disorder M-N (navigational concept) false Inferred relationship Some
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Familial multiple tumor syndrome false Inferred relationship Some
syndrome des hamartomes multiples (trouble) localisation d'une constatation (attribut) intestins true Inferred relationship Some 1
syndrome des hamartomes multiples (trouble) morphologie associée (attribut) polype true Inferred relationship Some 1
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Digestive system hereditary disorder true Inferred relationship Some
syndrome des hamartomes multiples (trouble) est un(e) (attribut) Congenital hamartoma (disorder) false Inferred relationship Some
syndrome des hamartomes multiples (trouble) survenue (attribut) congénital true Inferred relationship Some 2
syndrome des hamartomes multiples (trouble) morphologie associée (attribut) Hamartoma (morphologic abnormality) true Inferred relationship Some 2
syndrome des hamartomes multiples (trouble) morphologie associée (attribut) Hamartoma (morphologic abnormality) false Inferred relationship Some
syndrome des hamartomes multiples (trouble) localisation d'une constatation (attribut) intestins false Inferred relationship Some 1
syndrome des hamartomes multiples (trouble) survenue (attribut) congénital false Inferred relationship Some
syndrome des hamartomes multiples (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some
syndrome des hamartomes multiples (trouble) est un(e) (attribut) syndrome tumoral hamartomateux lié à PTEN true Inferred relationship Some
syndrome des hamartomes multiples (trouble) survenue (attribut) congénital true Inferred relationship Some 1
syndrome des hamartomes multiples (trouble) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Gingival enlargement due to Cowden syndrome Due to True syndrome des hamartomes multiples (trouble) Inferred relationship Some 2
Family history of Cowden syndrome (situation) constatation associée (attribut) True syndrome des hamartomes multiples (trouble) Inferred relationship Some 1

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

GB English

US English

Back to Start