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771339005: hyperzincémie et hypercalprotectinémie (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3705819013 Recurrent infection, inflammatory syndrome due to zinc metabolism disorder syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705820019 Hyperzincemia and hypercalprotectinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705821015 Hyperzincemia and hypercalprotectinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705822010 Hyperzincaemia and hypercalprotectinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
770631000241114 hyperzincémie et hypercalprotectinémie (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
913561000172118 syndrome d'infections récurrentes, syndrome inflammatoire par anomalie du métabolisme du zinc fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
987731000172110 hyperzincémie et hypercalprotectinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3705823017 A rare inborn error of zinc metabolism characterized by recurrent infections, hepatosplenomegaly, anemia (unresponsive to iron supplementation) and chronic systemic inflammation in the presence of high plasma concentrations of zinc and calprotectin. Patients typically present dermal ulcers or other cutaneous manifestations (for example inflammation) and arthralgia. Severe epistaxis and spontaneous hematomas have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3705824011 A rare inborn error of zinc metabolism characterised by recurrent infections, hepatosplenomegaly, anaemia (unresponsive to iron supplementation) and chronic systemic inflammation in the presence of high plasma concentrations of zinc and calprotectin. Patients typically present dermal ulcers or other cutaneous manifestations (for example inflammation) and arthralgia. Severe epistaxis and spontaneous haematomas have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperzincemia and hypercalprotectinemia (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Hyperzincemia and hypercalprotectinemia (disorder) est un(e) (attribut) Inflammatory disorder true Inferred relationship Some
Hyperzincemia and hypercalprotectinemia (disorder) morphologie associée (attribut) Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1
Hyperzincemia and hypercalprotectinemia (disorder) survenue (attribut) enfance true Inferred relationship Some 1
Hyperzincemia and hypercalprotectinemia (disorder) est un(e) (attribut) Disorder of zinc metabolism true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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