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65031000119108: Family history of Cowden syndrome (situation)

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

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 SNOMED CT core module
3438377016 Family history of Cowden syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of Cowden syndrome Is a Family history: Gastrointestinal disease false Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Is a Family history of congenital disease false Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Is a Family history of neoplasm false Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Is a Family history of hereditary disease true Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Associated finding Cowden syndrome true Inferred relationship Existential restriction modifier 1
Family history of Cowden syndrome Finding context Known present true Inferred relationship Existential restriction modifier 1
Family history of Cowden syndrome Temporal context Current or past true Inferred relationship Existential restriction modifier 1
Family history of Cowden syndrome Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier 1
Family history of Cowden syndrome Is a Family history: Skin disease true Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Is a Family history of multiple congenital anomalies true Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Is a Family history: Congenital gastrointestinal tract anomaly true Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Subject relationship context Person in the family true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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