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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 Reference Sets
124688012 Nemaline myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
124689016 Nemaline body disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
124690013 Rod myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
502903015 Rod-body myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
815641013 Nemaline myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
1457171000005116 Nemalin myopati da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept) Danish language reference set (foundation metadata concept): Preferred (foundation metadata concept)

2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nemaline myopathy Is a Congenital myopathy false Inferred relationship Some
Nemaline myopathy Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 1
Nemaline myopathy Is a Disorder of skeletal muscle false Inferred relationship Some
Nemaline myopathy Is a Congenital anomaly of skeletal muscle true Inferred relationship Some
Nemaline myopathy Occurrence Congenital false Inferred relationship Some
Nemaline myopathy Associated morphology kongenit anomali false Inferred relationship Some 1
Nemaline myopathy Finding site Skeletal muscle structure (body structure) true Inferred relationship Some 1
Nemaline myopathy Associated morphology kongenit anomali false Inferred relationship Some 1
Nemaline myopathy Occurrence Congenital false Inferred relationship Some 2
Nemaline myopathy Associated morphology dysgenese false Inferred relationship Some 2
Nemaline myopathy Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 2
Nemaline myopathy Occurrence Congenital true Inferred relationship Some 1
Nemaline myopathy Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Nemaline myopathy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Nemaline myopathy, early onset type Is a True Nemaline myopathy Inferred relationship Some
Nemaline myopathy, late onset type Is a True Nemaline myopathy Inferred relationship Some

Reference Sets

Danish translated concepts reference set (foundation metadata concept)

GB English

US English

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