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129621001: Nemaline myopathy, early onset 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
208442014 Nemaline myopathy, early onset type en Synonym Active Entire term case insensitive SNOMED CT core module
733777019 Nemaline myopathy, early onset type (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4695183010 Congenital nemaline myopathy en Synonym Active Entire term case insensitive SNOMED CT core module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nemaline myopathy, early onset type Is a Nemaline myopathy true Inferred relationship Existential restriction modifier
Nemaline myopathy, early onset type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, early onset type Occurrence Congenital false Inferred relationship Existential restriction modifier
Nemaline myopathy, early onset type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, early onset type Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Nemaline myopathy, early onset type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, early onset type Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Nemaline myopathy, early onset type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Nemaline myopathy, early onset type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Nemaline myopathy, early onset type Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, early onset type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Nemaline myopathy, early onset type Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, early onset type Is a Congenital disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Typical nemaline myopathy Is a True Nemaline myopathy, early onset type Inferred relationship Existential restriction modifier
Actin accumulation myopathy Is a True Nemaline myopathy, early onset type Inferred relationship Existential restriction modifier
Intermediate nemaline myopathy Is a True Nemaline myopathy, early onset type Inferred relationship Existential restriction modifier
Severe congenital nemaline myopathy Is a True Nemaline myopathy, early onset type Inferred relationship Existential restriction modifier
Amish nemaline myopathy Is a True Nemaline myopathy, early onset type Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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