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64971000119106: Family history of Von Hippel-Lindau syndrome (situation)


Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3466494017 Family history of Von Hippel-Lindau syndrome (situation) en Fully specified name Active Initial character case insensitive SNOMED CT core
3466495016 Family history of Von Hippel-Lindau syndrome en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of Von Hippel-Lindau syndrome Is a Family history of development disorder false Inferred relationship Some
Family history of Von Hippel-Lindau syndrome Is a FH: neoplasm of skin true Inferred relationship Some
Family history of Von Hippel-Lindau syndrome Subject relationship context Person in the family true Inferred relationship Some 1
Family history of Von Hippel-Lindau syndrome Is a FH: Skin disease false Inferred relationship Some
Family history of Von Hippel-Lindau syndrome Is a Family history of congenital disease true Inferred relationship Some
Family history of Von Hippel-Lindau syndrome Is a Family history of neurological disorder true Inferred relationship Some
Family history of Von Hippel-Lindau syndrome Is a Family history of hereditary disease true Inferred relationship Some
Family history of Von Hippel-Lindau syndrome Associated finding Von Hippel-Lindau syndrome true Inferred relationship Some 1
Family history of Von Hippel-Lindau syndrome Finding context Known present true Inferred relationship Some 1
Family history of Von Hippel-Lindau syndrome Temporal context Current or past true Inferred relationship Some 1
Family history of Von Hippel-Lindau syndrome Subject relationship context Person in family of subject false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

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