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37702000: Hereditary acrodermatitis enteropathica (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
423071000241117 acrodermatite entéropathique héréditaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
486788010 AE - Acrodermatitis enteropathica en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486789019 Primary zinc malabsorption en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
486790011 Danbolt-Close syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486791010 Acrodermatitis enteropathica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
50004071000188110 acrodermatite entéropathique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
62890013 Hereditary acrodermatitis enteropathica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62891012 Primary zinc malabsorption syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62892017 Brandt syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
62893010 Danbolt-Closs syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
62894016 Hereditary acrodermatitis enterohepatica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769600013 Hereditary acrodermatitis enteropathica (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
acrodermatite entéropathique héréditaire (trouble) morphologie associée (attribut) Papule false Inferred relationship Some 1
acrodermatite entéropathique héréditaire (trouble) est un(e) (attribut) Gianotti-Crosti syndrome true Inferred relationship Some
acrodermatite entéropathique héréditaire (trouble) est un(e) (attribut) Papule of skin (finding) false Inferred relationship Some
acrodermatite entéropathique héréditaire (trouble) localisation d'une constatation (attribut) Skin structure of extremity true Inferred relationship Some 2
acrodermatite entéropathique héréditaire (trouble) morphologie associée (attribut) Papular rash true Inferred relationship Some 2
acrodermatite entéropathique héréditaire (trouble) survenue (attribut) enfance true Inferred relationship Some 2
acrodermatite entéropathique héréditaire (trouble) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
acrodermatite entéropathique héréditaire (trouble) est un(e) (attribut) Acrodermatitis false Inferred relationship Some
acrodermatite entéropathique héréditaire (trouble) est un(e) (attribut) Disorder of zinc metabolism true Inferred relationship Some
acrodermatite entéropathique héréditaire (trouble) est un(e) (attribut) Hereditary disorder of the integument true Inferred relationship Some
acrodermatite entéropathique héréditaire (trouble) localisation d'une constatation (attribut) Skin structure of extremity false Inferred relationship Some 1
acrodermatite entéropathique héréditaire (trouble) localisation d'une constatation (attribut) Skin structure of extremity false Inferred relationship Some 1
acrodermatite entéropathique héréditaire (trouble) morphologie associée (attribut) inflammation false Inferred relationship Some 1
acrodermatite entéropathique héréditaire (trouble) morphologie associée (attribut) inflammation false Inferred relationship Some 1
acrodermatite entéropathique héréditaire (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
acrodermatite entéropathique héréditaire (trouble) morphologie associée (attribut) Papulovesicular rash false Inferred relationship Some
acrodermatite entéropathique héréditaire (trouble) localisation d'une constatation (attribut) structure d'un membre 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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