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240095001: Lipid storage myopathy (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
359705015 Lipid storage myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
629192012 Lipid storage myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lipid storage myopathy Is a Metabolic myopathy true Inferred relationship Existential restriction modifier
Lipid storage myopathy Is a Congenital anomaly of skeletal muscle false Inferred relationship Existential restriction modifier
Lipid storage myopathy Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Lipid storage myopathy Is a Lipid storage disease true Inferred relationship Existential restriction modifier
Lipid storage myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 2
Lipid storage myopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Neutral lipid storage disease with myopathy Is a True Lipid storage myopathy Inferred relationship Existential restriction modifier
Genetic recurrent myoglobinuria Is a True Lipid storage myopathy Inferred relationship Existential restriction modifier
Autosomal dominant myoglobinuria Is a True Lipid storage myopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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