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37702000: Hereditary acrodermatitis enteropathica (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
62890013 Hereditary acrodermatitis enteropathica en Synonym Active Entire term case insensitive SNOMED CT core module
62891012 Primary zinc malabsorption syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
62892017 Brandt syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
62893010 Danbolt-Closs syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
62894016 Hereditary acrodermatitis enterohepatica en Synonym Active Entire term case insensitive SNOMED CT core module
486788010 AE - Acrodermatitis enteropathica en Synonym Active Entire term case sensitive SNOMED CT core module
486789019 Primary zinc malabsorption en Synonym Active Entire term case insensitive SNOMED CT core module
486790011 Danbolt-Close syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
486791010 Acrodermatitis enteropathica en Synonym Active Entire term case insensitive SNOMED CT core module
769600013 Hereditary acrodermatitis enteropathica (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Hereditary acrodermatitis enteropathica Is a Acrodermatitis false Inferred relationship Existential restriction modifier
Hereditary acrodermatitis enteropathica Is a Disorder of zinc metabolism true Inferred relationship Existential restriction modifier
Hereditary acrodermatitis enteropathica Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Hereditary acrodermatitis enteropathica Associated morphology Inflammation false Inferred relationship Existential restriction modifier 1
Hereditary acrodermatitis enteropathica Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Hereditary acrodermatitis enteropathica Associated morphology Papulovesicular rash false Inferred relationship Existential restriction modifier
Hereditary acrodermatitis enteropathica Finding site Limb structure false Inferred relationship Existential restriction modifier
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity false Inferred relationship Existential restriction modifier 1
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity false Inferred relationship Existential restriction modifier 1
Hereditary acrodermatitis enteropathica Associated morphology Inflammation false Inferred relationship Existential restriction modifier 1
Hereditary acrodermatitis enteropathica Associated morphology Papule false Inferred relationship Existential restriction modifier 1
Hereditary acrodermatitis enteropathica Is a Gianotti-Crosti syndrome true Inferred relationship Existential restriction modifier
Hereditary acrodermatitis enteropathica Is a Papule of skin false Inferred relationship Existential restriction modifier
Hereditary acrodermatitis enteropathica Finding site Skin structure of extremity true Inferred relationship Existential restriction modifier 2
Hereditary acrodermatitis enteropathica Associated morphology Papular rash true Inferred relationship Existential restriction modifier 2
Hereditary acrodermatitis enteropathica Occurrence Childhood true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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