75072002: Nemaline myopathy (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Finding of power of skeletal muscle\Muscle weakness\Nemaline myopathy
\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Nemaline myopathy

\Muscle finding\Finding of power of skeletal muscle\Muscle weakness\Nemaline myopathy
\Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Nemaline myopathy

\Musculoskeletal finding\Finding of power of skeletal muscle\Muscle weakness\Nemaline myopathy
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal muscle\Nemaline myopathy

\Disease\Genetic disease\Nemaline myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Nemaline myopathy
\Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Nemaline myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Nemaline myopathy

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

124688012 Nemaline myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
124689016 Nemaline body disease en Synonym Active Entire term case insensitive SNOMED CT core module
124690013 Rod myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
502903015 Rod-body myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
815641013 Nemaline myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Nemaline myopathy	Is a	Congenital myopathy	false	Inferred relationship	Existential restriction modifier
Nemaline myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	1
Nemaline myopathy	Is a	Disorder of skeletal muscle	true	Inferred relationship	Existential restriction modifier
Nemaline myopathy	Is a	Congenital anomaly of skeletal muscle	false	Inferred relationship	Existential restriction modifier
Nemaline myopathy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Nemaline myopathy	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Nemaline myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1
Nemaline myopathy	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Nemaline myopathy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Nemaline myopathy	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Nemaline myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	2
Nemaline myopathy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	1
Nemaline myopathy	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier	1
Nemaline myopathy	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	1
Nemaline myopathy	Is a	Genetic disease	true	Inferred relationship	Existential restriction modifier
Nemaline myopathy	Is a	Muscle weakness	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Nemaline myopathy, early onset type	Is a	True	Nemaline myopathy	Inferred relationship	Existential restriction modifier
Nemaline myopathy, late onset type	Is a	True	Nemaline myopathy	Inferred relationship	Existential restriction modifier
Childhood-onset nemaline myopathy	Is a	True	Nemaline myopathy	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets