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718572004: Bethlem myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3312733011 Bethlem myopathy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3312803013 Bethlem myopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3312804019 Benign autosomal dominant myopathy en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bethlem myopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Bethlem myopathy Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier
Bethlem myopathy Is a Hereditary progressive muscular dystrophy false Inferred relationship Existential restriction modifier
Bethlem myopathy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Bethlem myopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Bethlem myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Bethlem myopathy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 3
Bethlem myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Bethlem myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Bethlem myopathy Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
Bethlem myopathy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Bethlem myopathy Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Bethlem myopathy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Bethlem myopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Bethlem myopathy Clinical course Progressive true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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