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1003938005: Phenylketonuria due to tetrahydrobiopterin deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4167012011 Phenylketonuria due to BH4 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4167014012 Phenylketonuria due to tetrahydrobiopterin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4167524012 Phenylketonuria due to tetrahydrobiopterin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Phenylketonuria due to tetrahydrobiopterin deficiency est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Phenylketonuria due to tetrahydrobiopterin deficiency est un(e) (attribut) Hyperphenylalaninemia false Inferred relationship Some
Phenylketonuria due to tetrahydrobiopterin deficiency Due to Disorder of tetrahydrobiopterin metabolism true Inferred relationship Some 1
Phenylketonuria due to tetrahydrobiopterin deficiency est un(e) (attribut) Phenylketonuria (disorder) true Inferred relationship Some
Phenylketonuria due to tetrahydrobiopterin deficiency survenue (attribut) congénital true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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