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240085008: Congenital myopathy with uniform fiber type (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
359690011 Congenital myopathy with uniform fiber type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core US English: Preferred (foundation metadata concept)
359691010 Congenital myopathy with uniform fibre type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
629179014 Congenital myopathy with uniform fiber type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
1457121000005117 kongenit myopati med ensartet fibertype 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)

0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Danish translated concepts reference set (foundation metadata concept)

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