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56595005: Hypertyrosinemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
94117019 Hypertyrosinemia en Synonym Active Entire term case insensitive SNOMED CT core module
94119016 Elevated tyrosine blood level en Synonym Active Entire term case insensitive SNOMED CT core module
497657013 Hypertyrosinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
795124017 Hypertyrosinemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertyrosinemia Is a Disorder of tyrosine metabolism true Inferred relationship Existential restriction modifier
Hypertyrosinemia Is a Aminoacidemia true Inferred relationship Existential restriction modifier
Hypertyrosinemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Hypertyrosinemia Occurrence Congenital false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary hypertyrosinemia Is a True Hypertyrosinemia Inferred relationship Existential restriction modifier
Hypertyrosinemia, Richner-Hanhart type Is a False Hypertyrosinemia Inferred relationship Existential restriction modifier
Transient neonatal hypertyrosinemia Is a True Hypertyrosinemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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