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770792007: Adult-onset distal myopathy due to valosin containing protein mutation (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3702811017 Adult-onset distal myopathy due to VCP (valosin containing protein) mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
3702812012 Adult-onset distal myopathy due to valosin containing protein mutation (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3702813019 Adult-onset distal myopathy due to VCP mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
3702814013 Adult-onset distal myopathy due to valosin containing protein mutation 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
Adult-onset distal myopathy due to valosin containing protein mutation Occurrence Adulthood true Inferred relationship Existential restriction modifier 1
Adult-onset distal myopathy due to valosin containing protein mutation Is a Hereditary progressive muscular dystrophy false Inferred relationship Existential restriction modifier
Adult-onset distal myopathy due to valosin containing protein mutation Is a Distal muscular dystrophy true Inferred relationship Existential restriction modifier
Adult-onset distal myopathy due to valosin containing protein mutation Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Adult-onset distal myopathy due to valosin containing protein mutation Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Adult-onset distal myopathy due to valosin containing protein mutation Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Adult-onset distal myopathy due to valosin containing protein mutation Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Adult-onset distal myopathy due to valosin containing protein mutation Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Adult-onset distal myopathy due to valosin containing protein mutation Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 2
Adult-onset distal myopathy due to valosin containing protein mutation Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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