770787005: Benign Samaritan congenital myopathy (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy

\Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy

\Musculoskeletal finding\Disorder of musculoskeletal system\...

\Hereditary disorder of musculoskeletal system\Benign congenital myopathy\Benign Samaritan congenital myopathy

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Benign Samaritan congenital myopathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Developmental disorder\Developmental hereditary disorder\Benign congenital myopathy\Benign Samaritan congenital myopathy
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy\Benign Samaritan congenital myopathy

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3702794016 Benign Samaritan congenital myopathy (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3702795015 Benign Samaritan congenital myopathy en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign Samaritan congenital myopathy	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Benign Samaritan congenital myopathy	Is a	Benign congenital myopathy	true	Inferred relationship	Existential restriction modifier
Benign Samaritan congenital myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1
Benign Samaritan congenital myopathy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Benign Samaritan congenital myopathy	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Benign Samaritan congenital myopathy	Pathological process	Pathological developmental process	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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Id	Description	Lang	Type	Status	Case?	Module
3702794016	Benign Samaritan congenital myopathy (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3702795015	Benign Samaritan congenital myopathy	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module