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415764005: Tyrosinemia type III (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2530083018 Tyrosinemia type III (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2533519017 Tyrosinemia type III en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2533520011 Tyrosinaemia type III en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3035359011 Tyrosinemia type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035481017 Tyrosinaemia type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5314213014 HPD-gene related tyrosinemia type III en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5314214015 HPD-gene related tyrosinaemia type III en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2530083018 Tyrosinemia type III (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2533519017 Tyrosinemia type III en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2533520011 Tyrosinaemia type III en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3035359011 Tyrosinemia type 3 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3035359011 Tyrosinemia type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035481017 Tyrosinaemia type 3 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3035481017 Tyrosinaemia type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5314213014 HPD-gene related tyrosinemia type III en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5314214015 HPD-gene related tyrosinaemia type III en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3408621001000114 Tyrosinämie Typ 3 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
907951000172119 tyrosinémie type 3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
955121000172110 tyrosinémie par déficit en 4-hydroxyphénylpyruvate dioxygénase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
907951000172119 tyrosinémie type 3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
955121000172110 tyrosinémie par déficit en 4-hydroxyphénylpyruvate dioxygénase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3408621001000114 Tyrosinämie Typ 3 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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