1197156008: Intermediate nemaline myopathy (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Finding of power of skeletal muscle\Muscle weakness\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy
\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy

\Muscle finding\Finding of power of skeletal muscle\Muscle weakness\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy
\Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy

\Musculoskeletal finding\Finding of power of skeletal muscle\Muscle weakness\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Intermediate nemaline myopathy
\Musculoskeletal finding\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Intermediate nemaline myopathy
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal muscle\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy

\Disease\Genetic disease\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Intermediate nemaline myopathy
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Intermediate nemaline myopathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Intermediate nemaline myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Intermediate nemaline myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Intermediate nemaline myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy
\Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy
\Disease\Congenital disease\Nemaline myopathy, early onset type\Intermediate nemaline myopathy
\Disease\Chronic disease\Chronic disease of musculoskeletal system\Intermediate nemaline myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Nemaline myopathy\Nemaline myopathy, early onset type\Intermediate nemaline myopathy

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

4695208013 Intermediate nemaline myopathy en Synonym Active Entire term case insensitive SNOMED CT core module

4695209017 Intermediate 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
Intermediate nemaline myopathy	Is a	Chronic disease of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Intermediate nemaline myopathy	Is a	Nemaline myopathy, early onset type	true	Inferred relationship	Existential restriction modifier
Intermediate nemaline myopathy	Is a	Autosomal hereditary disorder	true	Inferred relationship	Existential restriction modifier
Intermediate nemaline myopathy	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Intermediate nemaline myopathy	Clinical course	Progressive	true	Inferred relationship	Existential restriction modifier	2
Intermediate nemaline myopathy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Intermediate nemaline myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets