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702382000: Inclusion body myopathy 2 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2995199011 Hereditary inclusion body myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
2995276019 Inclusion body myopathy 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2995349016 Rimmed vacuole myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
2995564015 Inclusion body myopathy 2 en Synonym Active Entire term case insensitive SNOMED CT core module
2995724017 Distal myopathy with rimmed vacuoles en Synonym Active Entire term case insensitive SNOMED CT core module
2995749018 Quadricep sparing inclusion body myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
2995887019 Nonaka myopathy 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
Inclusion body myopathy 2 Is a Myopathy with cytoplasmic inclusions true Inferred relationship Existential restriction modifier
Inclusion body myopathy 2 Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Inclusion body myopathy 2 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Inclusion body myopathy 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Inclusion body myopathy 2 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Inclusion body myopathy 2 Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Inclusion body myopathy 2 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Inclusion body myopathy 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Inclusion body myopathy 2 Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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