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64161000119102: Family history of phenylketonuria (situation)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3043581018 Family history of phenylketonuria en Synonym Active Entire term case insensitive SNOMED CT core module
3043641019 Family history of phenylketonuria (situation) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of phenylketonuria Is a Family history of congenital disease true Inferred relationship Existential restriction modifier
Family history of phenylketonuria Is a Family history of metabolic disorder true Inferred relationship Existential restriction modifier
Family history of phenylketonuria Is a Family history of hereditary disease true Inferred relationship Existential restriction modifier
Family history of phenylketonuria Associated finding Classical phenylketonuria true Inferred relationship Existential restriction modifier 1
Family history of phenylketonuria Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier 1
Family history of phenylketonuria Temporal context Current or past true Inferred relationship Existential restriction modifier 1
Family history of phenylketonuria Finding context Known present true Inferred relationship Existential restriction modifier 1
Family history of phenylketonuria 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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