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240082006: Myopathy with abnormality of histochemical 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
359685013 Myopathy with abnormality of histochemical fibre type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
359686014 Myopathy with abnormality of histochemical fiber type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core Danish translated concepts reference set (foundation metadata concept)
629176019 Myopathy with abnormality of histochemical fiber type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
1457101000005113 myopati med abnorm histokemisk 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)

3 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Myopathy with type I hypotrophy Is a True Myopathy with abnormality of histochemical fibre type Inferred relationship Some
Congenital myopathy with fibre type disproportion Is a True Myopathy with abnormality of histochemical fibre type Inferred relationship Some
Congenital myopathy with uniform fiber type Is a True Myopathy with abnormality of histochemical fibre type Inferred relationship Some

Reference Sets

Danish translated concepts reference set (foundation metadata concept)

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