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37702000: acrodermatitis enteropathica (aandoening)


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
347201000146115 acrodermatitis enteropathica nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
347211000146118 acrodermatitis enteropathica (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7584081000146116 Dit is een stofwisselingsaandoening die gepaard gaat met huiduitslag, haaruitval en diarree. De oorzaak is een tekort aan zink. nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


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 Some
Hereditary acrodermatitis enteropathica Is a acrodermatitis (aandoening) false Inferred relationship Some
Hereditary acrodermatitis enteropathica Is a Disorder of zinc metabolism true Inferred relationship Some
Hereditary acrodermatitis enteropathica Is a Hereditary disorder of the integument true Inferred relationship Some
Hereditary acrodermatitis enteropathica Associated morphology ontsteking (afwijkende morfologie) false Inferred relationship Some 1
Hereditary acrodermatitis enteropathica Finding site Skin structure false Inferred relationship Some 1
Hereditary acrodermatitis enteropathica Associated morphology Papulovesicular rash false Inferred relationship Some
Hereditary acrodermatitis enteropathica Finding site Limb structure false Inferred relationship Some
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity false Inferred relationship Some 1
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity false Inferred relationship Some 1
Hereditary acrodermatitis enteropathica Associated morphology ontsteking (afwijkende morfologie) false Inferred relationship Some 1
Hereditary acrodermatitis enteropathica Associated morphology Papule false Inferred relationship Some 1
Hereditary acrodermatitis enteropathica Is a Gianotti-Crosti syndrome true Inferred relationship Some
Hereditary acrodermatitis enteropathica Is a Papule of skin false Inferred relationship Some
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity true Inferred relationship Some 2
Hereditary acrodermatitis enteropathica Associated morphology Papular rash true Inferred relationship Some 2
Hereditary acrodermatitis enteropathica Occurrence Childhood true Inferred relationship Some 2
Hereditary acrodermatitis enteropathica Is a Hereditary metabolic disease false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Dutch pathology simple reference set (foundation metadata concept)

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