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75072002: Nemaline myopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
124688012 Nemaline myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
124689016 Nemaline body disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
124690013 Rod myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502903015 Rod-body myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
815641013 Nemaline myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
124688012 Nemaline myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
124688012 Nemaline myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
124689016 Nemaline body disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
124689016 Nemaline body disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
124690013 Rod myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
124690013 Rod myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502903015 Rod-body myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
502903015 Rod-body myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
815641013 Nemaline myopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
815641013 Nemaline myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3421751001000114 Nemalin-Myopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
919491000172114 myopathie congénitale à bâtonnets fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
926621000172111 myopathie à némaline fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
919491000172114 myopathie congénitale à bâtonnets fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
926621000172111 myopathie à némaline fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3421751001000114 Nemalin-Myopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nemaline myopathy (disorder) Is a Congenital myopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Nemaline myopathy (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nemaline myopathy (disorder) Is a Disorder of skeletal muscle true Inferred relationship Existential restriction modifier (core metadata concept)
Nemaline myopathy (disorder) Is a Congenital anomaly of skeletal muscle (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Nemaline myopathy (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Nemaline myopathy (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nemaline myopathy (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Nemaline myopathy (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nemaline myopathy (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Nemaline myopathy (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Nemaline myopathy (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Nemaline myopathy (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nemaline myopathy (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nemaline myopathy (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nemaline myopathy (disorder) Is a Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Nemaline myopathy (disorder) Is a Muscle weakness true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Nemaline myopathy, early onset type Is a True Nemaline myopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Nemaline myopathy, late onset type Is a True Nemaline myopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset nemaline myopathy Is a True Nemaline myopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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