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699315005: Neutral lipid storage disease with myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983780011 Neutral lipid storage disease with myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983783013 Neutral lipid storage disease with myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neutral lipid storage disease with myopathy (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Neutral lipid storage disease with myopathy (disorder) Is a Lipid storage myopathy true Inferred relationship Some
Neutral lipid storage disease with myopathy (disorder) Occurrence Congenital true Inferred relationship Some 2
Neutral lipid storage disease with myopathy (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Neutral lipid storage disease with myopathy (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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