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699315005: Neutral lipid storage disease with myopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

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


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 Some
Neutral lipid storage disease with myopathy Is a Lipid storage myopathy true Inferred relationship Some
Neutral lipid storage disease with myopathy Occurrence Congenital true Inferred relationship Some 2
Neutral lipid storage disease with myopathy Finding site Skeletal muscle structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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