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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
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
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
769600013 Hereditary acrodermatitis enteropathica (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
62890013 Hereditary acrodermatitis enteropathica en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character case insensitive (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
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 Only initial character case insensitive (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 Only initial character case insensitive (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
769600013 Hereditary acrodermatitis enteropathica (disorder) en Fully specified name Active Only initial character 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
3453431001000111 Acrodermatitis enteropathica de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50004071000188110 acrodermatite entéropathique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50004071000188110 acrodermatite entéropathique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3453431001000111 Acrodermatitis enteropathica 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
Hereditary acrodermatitis enteropathica Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Is a acrodermatite false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Is a Disorder of zinc metabolism (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary acrodermatitis enteropathica Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary acrodermatitis enteropathica Associated morphology Papulovesicular rash false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary acrodermatitis enteropathica Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary acrodermatitis enteropathica Associated morphology A small, solid lesion, less than 1 cm in diameter, raised above the surface of the surrounding skin and hence palpable false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary acrodermatitis enteropathica Is a Gianotti-Crosti syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Is a Papule of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary acrodermatitis enteropathica Associated morphology Papular rash true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary acrodermatitis enteropathica Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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