1197155007: Amish 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\Amish nemaline myopathy
\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Nemaline myopathy\Nemaline myopathy, early onset type\Amish nemaline myopathy

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

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

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

4695201019 Amish nemaline myopathy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

4695202014 Amish nemaline myopathy en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Amish nemaline myopathy	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Amish nemaline myopathy	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Amish nemaline myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1
Amish nemaline myopathy	Is a	Nemaline myopathy, early onset type	true	Inferred relationship	Existential restriction modifier
Amish nemaline myopathy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

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This concept is not in any reference sets