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65031000119108: Family history of Cowden syndrome (situation)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3438376013 Family history of Cowden syndrome (situation) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3438377016 Family history of Cowden syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of Cowden syndrome (situation) est un(e) (attribut) FH: Congenital GIT anomaly true Inferred relationship Some
Family history of Cowden syndrome (situation) est un(e) (attribut) FH: Gastrointestinal disease false Inferred relationship Some
Family history of Cowden syndrome (situation) est un(e) (attribut) Family history of congenital disease (situation) false Inferred relationship Some
Family history of Cowden syndrome (situation) est un(e) (attribut) Family history of neoplasm (situation) false Inferred relationship Some
Family history of Cowden syndrome (situation) est un(e) (attribut) Family history of hereditary disease (situation) true Inferred relationship Some
Family history of Cowden syndrome (situation) constatation associée (attribut) syndrome des hamartomes multiples (trouble) true Inferred relationship Some 1
Family history of Cowden syndrome (situation) contexte de la constatation (attribut) présence connue true Inferred relationship Some 1
Family history of Cowden syndrome (situation) contexte temporel (attribut) actuel ou passé true Inferred relationship Some 1
Family history of Cowden syndrome (situation) nature de la relation avec la personne visée (attribut) Person in family of subject (person) true Inferred relationship Some 1
Family history of Cowden syndrome (situation) est un(e) (attribut) FH: Skin disease true Inferred relationship Some
Family history of Cowden syndrome (situation) est un(e) (attribut) Family history of multiple congenital anomalies (situation) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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