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699315005: Neutral lipid storage disease with myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2983772016 Neutral lipid storage disease without ichthyosis en Synonym Active Entire term case insensitive SNOMED CT core module
2983780011 Neutral lipid storage disease with myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2983783013 Neutral lipid storage disease with myopathy en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neutral lipid storage disease with myopathy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Neutral lipid storage disease with myopathy Is a Lipid storage myopathy true Inferred relationship Existential restriction modifier
Neutral lipid storage disease with myopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Neutral lipid storage disease with myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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