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715317001: Proximal myotonic myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3302203011 Proximal myotonic myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302204017 Proximal myotonic myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3302205016 Myotonic dystrophy type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
3302206015 Ricker disease en Synonym Active Entire term case sensitive SNOMED CT core module
3302207012 Ricker syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Proximal myotonic myopathy Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Proximal myotonic myopathy Is a Myotonic disorder false Inferred relationship Existential restriction modifier
Proximal myotonic myopathy Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Proximal myotonic myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Proximal myotonic myopathy Is a Myotonic dystrophy true Inferred relationship Existential restriction modifier
Proximal myotonic myopathy Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Proximal myotonic myopathy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Proximal myotonic myopathy Pathological process Pathological developmental process 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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