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129622008: Nemaline myopathy, late 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
208443016 Nemaline myopathy, late onset type en Synonym Active Entire term case insensitive SNOMED CT core module
733778012 Nemaline myopathy, late onset type (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4695200018 Adult-onset nemaline myopathy en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nemaline myopathy, late onset type Is a Nemaline myopathy true Inferred relationship Existential restriction modifier
Nemaline myopathy, late onset type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Occurrence Congenital false Inferred relationship Existential restriction modifier
Nemaline myopathy, late onset type Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Nemaline myopathy, late onset type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Nemaline myopathy, late onset type Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Nemaline myopathy, late onset type Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Occurrence Adulthood true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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