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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
359685013 Myopathy with abnormality of histochemical fibre type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
359686014 Myopathy with abnormality of histochemical fiber type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629176019 Myopathy with abnormality of histochemical fiber type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
359685013 Myopathy with abnormality of histochemical fibre type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
359685013 Myopathy with abnormality of histochemical fibre type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
359686014 Myopathy with abnormality of histochemical fiber type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
359686014 Myopathy with abnormality of histochemical fiber type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629176019 Myopathy with abnormality of histochemical fiber type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
629176019 Myopathy with abnormality of histochemical fiber type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5036611000241118 myopathie avec anomalie des fibres de type histochimique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5036611000241118 myopathie avec anomalie des fibres de type histochimique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

15 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 Existential restriction modifier (core metadata concept)
Myopathy with abnormality of histochemical fibre type Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with abnormality of histochemical fibre type Is a Congenital anomaly of skeletal muscle (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Myopathy with abnormality of histochemical fibre type Finding site Skeletal muscle system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Myopathy with abnormality of histochemical fibre type Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with abnormality of histochemical fibre type Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Myopathy with abnormality of histochemical fibre type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with abnormality of histochemical fibre type Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with abnormality of histochemical fibre type Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Myopathy with abnormality of histochemical fibre type Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Myopathy with abnormality of histochemical fibre type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Myopathy with abnormality of histochemical fibre type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with abnormality of histochemical fibre type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with abnormality of histochemical fibre type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Myopathy with type I hypotrophy (disorder) Is a True Myopathy with abnormality of histochemical fibre type Inferred relationship Existential restriction modifier (core metadata concept)
Congenital myopathy with fibre type disproportion Is a True Myopathy with abnormality of histochemical fibre type Inferred relationship Existential restriction modifier (core metadata concept)
Congenital myopathy with uniform fiber type (disorder) Is a True Myopathy with abnormality of histochemical fibre type Inferred relationship Existential restriction modifier (core metadata concept)
Congenital myopathy with reduced type 2 muscle fibers (disorder) Is a True Myopathy with abnormality of histochemical fibre type Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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