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723579009: Tangier disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3425161019 Tangier disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3425162014 Tangier disease en Synonym Active Entire term case sensitive SNOMED CT core module
3425163016 Defective adenosine triphosphate-binding cassette transporter A1 en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Tangier disease Is a Familial lipoprotein deficiency true Inferred relationship Existential restriction modifier
Tangier disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Tangier disease Is a Lipoprotein deficiency disorder true Inferred relationship Existential restriction modifier
Tangier disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Autonomic neuropathy due to Tangier disease Due to True Tangier disease Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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