415764005: Tyrosinemia type III (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Tyrosinemia type III

\Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\4-Hydroxyphenylpyruvate dioxygenase deficiency\Tyrosinemia type III
\Metabolic disease\Enzymopathy\4-Hydroxyphenylpyruvate dioxygenase deficiency\Tyrosinemia type III

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

2530083018 Tyrosinemia type III (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

2533519017 Tyrosinemia type III en Synonym Active Only initial character case insensitive SNOMED CT core module

2533520011 Tyrosinaemia type III en Synonym Active Only initial character case insensitive SNOMED CT core module

3035359011 Tyrosinemia type 3 en Synonym Active Entire term case insensitive SNOMED CT core module

3035481017 Tyrosinaemia type 3 en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Tyrosinemia type III	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Tyrosinemia type III	Is a	4-Hydroxyphenylpyruvate dioxygenase deficiency	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets