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240082006: Myopathy with abnormality of histochemical fiber type (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
359685013 Myopathy with abnormality of histochemical fibre type en Synonym Active Entire term case insensitive SNOMED CT core module
359686014 Myopathy with abnormality of histochemical fiber type en Synonym Active Entire term case insensitive SNOMED CT core module
629176019 Myopathy with abnormality of histochemical fiber type (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

15 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myopathy with abnormality of histochemical fiber type Is a Congenital myopathy false Inferred relationship Existential restriction modifier
Myopathy with abnormality of histochemical fiber type Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Myopathy with abnormality of histochemical fiber type Is a Congenital anomaly of skeletal muscle true Inferred relationship Existential restriction modifier
Myopathy with abnormality of histochemical fiber type Finding site Skeletal muscle system structure false Inferred relationship Existential restriction modifier
Myopathy with abnormality of histochemical fiber type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Myopathy with abnormality of histochemical fiber type Occurrence Congenital false Inferred relationship Existential restriction modifier
Myopathy with abnormality of histochemical fiber type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Myopathy with abnormality of histochemical fiber type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Myopathy with abnormality of histochemical fiber type Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Myopathy with abnormality of histochemical fiber type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Myopathy with abnormality of histochemical fiber type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Myopathy with abnormality of histochemical fiber type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Myopathy with abnormality of histochemical fiber type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Myopathy with abnormality of histochemical fiber type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Myopathy with type I hypotrophy Is a True Myopathy with abnormality of histochemical fiber type Inferred relationship Existential restriction modifier
Congenital myopathy with fiber type disproportion Is a True Myopathy with abnormality of histochemical fiber type Inferred relationship Existential restriction modifier
Congenital myopathy with uniform fiber type Is a True Myopathy with abnormality of histochemical fiber type Inferred relationship Existential restriction modifier
Congenital myopathy with reduced type 2 muscle fibers Is a True Myopathy with abnormality of histochemical fiber type Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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