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30287008: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (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
1216334015 HHH - Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1217833013 HHH - Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
415021000241113 syndrome d'hyperornithinémie-hyperammoniémie-homocitrullinurie (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
484534018 Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
50692013 Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
761274013 Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
877751000172116 déficit en ORNT1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
956391000172116 syndrome d'hyperornithinémie-hyperammoniémie-homocitrullinurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
syndrome d'hyperornithinémie-hyperammoniémie-homocitrullinurie (trouble) est un(e) (attribut) Hyperammonemia true Inferred relationship Some
syndrome d'hyperornithinémie-hyperammoniémie-homocitrullinurie (trouble) est un(e) (attribut) trouble du métabolisme de l'ornithine true Inferred relationship Some
syndrome d'hyperornithinémie-hyperammoniémie-homocitrullinurie (trouble) est un(e) (attribut) Hyperornithinaemia true Inferred relationship Some
syndrome d'hyperornithinémie-hyperammoniémie-homocitrullinurie (trouble) survenue (attribut) congénital false Inferred relationship Some
syndrome d'hyperornithinémie-hyperammoniémie-homocitrullinurie (trouble) localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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