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297225000: Maternal phenylketonuria (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
437707011 Maternal phenylketonuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
692533018 Maternal phenylketonuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5314321018 PAH-gene related maternal phenylketonuria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5314322013 Maternal PKU (phenylketonuria) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
437707011 Maternal phenylketonuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
437707011 Maternal phenylketonuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
692533018 Maternal phenylketonuria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
692533018 Maternal phenylketonuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5314321018 PAH-gene related maternal phenylketonuria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5314322013 Maternal PKU (phenylketonuria) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3410781001000116 Phenylketonurie, maternale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929371000172114 embryopathie hyperphénylalaninémique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
939721000172114 phénylcétonurie maternelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929371000172114 embryopathie hyperphénylalaninémique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
939721000172114 phénylcétonurie maternelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3410781001000116 Phenylketonurie, maternale 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
Maternal phenylketonuria Is a Disorder of phenylalanine metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Maternal phenylketonuria Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Maternal phenylketonuria Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Maternal phenylketonuria Is a Autosomal recessive hereditary 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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